rs121913314

Orientation

plus

Stabilized

plus

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

Make rs121913314(C;T)

Make rs121913314(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

37403359

Gene

SRC

is a	snp
is	mentioned by
dbSNP	rs121913314
dbSNP (classic)	rs121913314
ClinGen	rs121913314
ebi	rs121913314
HLI	rs121913314
Exac	rs121913314
Gnomad	rs121913314
Varsome	rs121913314
LitVar	rs121913314
Map	rs121913314
PheGenI	rs121913314
Biobank	rs121913314
1000 genomes	rs121913314
hgdp	rs121913314
ensembl	rs121913314
geneview	rs121913314
scholar	rs121913314
google	rs121913314
pharmgkb	rs121913314
gwascentral	rs121913314
openSNP	rs121913314
23andMe	rs121913314
SNPshot	rs121913314
SNPdbe	rs121913314
MSV3d	rs121913314
GWAS Ctlg	rs121913314

Max Magnitude

0

OMIM	190090
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121913314(T;T)
Alt	rs121913314(T;T)
Reference	Rs121913314(C;C)
Significance	Pathogenic
Disease	Colon cancer Neoplasm
Variation	info
Gene	SRC
CLNDBN	Colon cancer, advanced Neoplasm
Reversed	0
HGVS	NC_000020.10:g.36031762C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013401.27, RCV000428592.1,

[PMID 32253932] Linkage disequilibrium and haplotype analysis of Src and Yes1 genes in thyroid cancer.