rs121913357

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common genotype
(G;G)	0	common in clinvar

Make rs121913357(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

140781603

Gene

BRAF

is a	snp
is	mentioned by
dbSNP	rs121913357
dbSNP (classic)	rs121913357
ClinGen	rs121913357
ebi	rs121913357
HLI	rs121913357
Exac	rs121913357
Gnomad	rs121913357
Varsome	rs121913357
LitVar	rs121913357
Map	rs121913357
PheGenI	rs121913357
Biobank	rs121913357
1000 genomes	rs121913357
hgdp	rs121913357
ensembl	rs121913357
geneview	rs121913357
scholar	rs121913357
google	rs121913357
pharmgkb	rs121913357
gwascentral	rs121913357
openSNP	rs121913357
23andMe	rs121913357
SNPshot	rs121913357
SNPdbe	rs121913357
MSV3d	rs121913357
GWAS Ctlg	rs121913357

Max Magnitude

0

OMIM	164757
Desc
Variant	0009
Related	also

ClinVar
Risk	Rs121913357(A;A) rs121913357(C;C) rs121913357(T;T)
Alt	Rs121913357(A;A) rs121913357(C;C) rs121913357(T;T)
Reference	Rs121913357(G;G)
Significance	Pathogenic
Disease	not specified Malignant lymphoma not provided Colorectal Neoplasms Squamous cell carcinoma of the skin Malignant melanoma Malignant melanoma of skin Transitional cell carcinoma of the bladder Multiple myeloma Adenocarcinoma of prostate Adenocarcinoma of lung Squamous cell carcinoma of lung Non-small cell lung cancer
Variation	info
Gene	BRAF
CLNDBN	not specified Malignant lymphoma, non-Hodgkin not provided Colorectal Neoplasms Squamous cell carcinoma of the skin Malignant melanoma Malignant melanoma of skin Transitional cell carcinoma of the bladder Multiple myeloma Adenocarcinoma of prostate Adenocarcinoma of lung Squamous cell carcinoma of lung Non-small cell lung cancer
Reversed	1
HGVS	NC_000007.13:g.140481403C>A; NC_000007.13:g.140481403C>G; NC_000007.13:g.140481403C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000150211.1, RCV000015004.8, RCV000033306.4, RCV000421772.1, RCV000422506.1, RCV000423124.1, RCV000428425.1, RCV000428973.1, RCV000433203.1, RCV000439076.1, RCV000439657.1, RCV000441999.1, RCV000154398.1, RCV000433832.1,