rs1057519955

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs1057519955(C;T)

Make rs1057519955(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

218584682

Gene

CNOT9

is a	snp
is	mentioned by
dbSNP	rs1057519955
dbSNP (classic)	rs1057519955
ClinGen	rs1057519955
ebi	rs1057519955
HLI	rs1057519955
Exac	rs1057519955
Gnomad	rs1057519955
Varsome	rs1057519955
LitVar	rs1057519955
Map	rs1057519955
PheGenI	rs1057519955
Biobank	rs1057519955
1000 genomes	rs1057519955
hgdp	rs1057519955
ensembl	rs1057519955
geneview	rs1057519955
scholar	rs1057519955
google	rs1057519955
pharmgkb	rs1057519955
gwascentral	rs1057519955
openSNP	rs1057519955
23andMe	rs1057519955
SNPshot	rs1057519955
SNPdbe	rs1057519955
MSV3d	rs1057519955
GWAS Ctlg	rs1057519955

Max Magnitude

0

ClinVar
Risk	rs1057519955(T;T)
Alt	rs1057519955(T;T)
Reference	Rs1057519955(C;C)
Significance	Probable-Pathogenic
Disease	Malignant melanoma of skin
Variation	info
Gene	RQCD1 CNOT9
CLNDBN	Malignant melanoma of skin
Reversed	0
HGVS	NC_000002.11:g.219449405C>T
CLNSRC
CLNACC	RCV000439915.1,