rs17217772

plus

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

Make rs17217772(A;G)

Make rs17217772(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47410107

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs17217772
dbSNP (classic)	rs17217772
ClinGen	rs17217772
ebi	rs17217772
HLI	rs17217772
Exac	rs17217772
Gnomad	rs17217772
Varsome	rs17217772
LitVar	rs17217772
Map	rs17217772
PheGenI	rs17217772
Biobank	rs17217772
1000 genomes	rs17217772
hgdp	rs17217772
ensembl	rs17217772
geneview	rs17217772
scholar	rs17217772
google	rs17217772
pharmgkb	rs17217772
gwascentral	rs17217772
openSNP	rs17217772
23andMe	rs17217772
SNPshot	rs17217772
SNPdbe	rs17217772
MSV3d	rs17217772
GWAS Ctlg	rs17217772

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

[PMID 25134804 ] Gly322Asp and Asn127Ser single nucleotide polymorphisms (SNPs) of hMSH2 mismatch repair gene and the risk of triple-negative breast cancer in Polish women

ClinVar
Risk	rs17217772(G;G) rs17217772(T;T)
Alt	rs17217772(G;G) rs17217772(T;T)
Reference	Rs17217772(A;A)
Significance	Non-pathogenic
Disease	Lynch syndrome not specified Lynch syndrome I Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome not specified Lynch syndrome I Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47637246A>G; NC_000002.11:g.47637246A>T
CLNSRC	HGMD UniProtKB (protein)
CLNACC	RCV000030253.4, RCV000035361.8, RCV000144619.1, RCV000162398.1, RCV000076589.2,