rs121908698

Orientation

minus

Stabilized

minus

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

Make rs121908698(G;T)

Make rs121908698(T;T)

Reference

GRCh38 38.1/142

Chromosome

22

Position

28725242

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs121908698
dbSNP (classic)	rs121908698
ClinGen	rs121908698
ebi	rs121908698
HLI	rs121908698
Exac	rs121908698
Gnomad	rs121908698
Varsome	rs121908698
LitVar	rs121908698
Map	rs121908698
PheGenI	rs121908698
Biobank	rs121908698
1000 genomes	rs121908698
hgdp	rs121908698
ensembl	rs121908698
geneview	rs121908698
scholar	rs121908698
google	rs121908698
pharmgkb	rs121908698
gwascentral	rs121908698
openSNP	rs121908698
23andMe	rs121908698
SNPshot	rs121908698
SNPdbe	rs121908698
MSV3d	rs121908698
GWAS Ctlg	rs121908698

Max Magnitude

0

ClinVar
Risk	rs121908698(A;A) rs121908698(T;T)
Alt	rs121908698(A;A) rs121908698(T;T)
Reference	Rs121908698(G;G)
Significance	Other
Disease	not provided Familial cancer of breast Hereditary cancer-predisposing syndrome Breast and colorectal cancer
Variation	info
Gene	CHEK2
CLNDBN	not provided Familial cancer of breast Hereditary cancer-predisposing syndrome Breast and colorectal cancer, susceptibility to
Reversed	1
HGVS	NC_000022.10:g.29121230C>A; NC_000022.10:g.29121230C>T
CLNSRC	ClinVar Ambry Genetics GeneDx
CLNACC	RCV000114770.3, RCV000199852.1, RCV000116017.8, RCV000196718.4, RCV000210090.1, RCV000212418.2,