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rs17217772

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs17217772(A;G)
Make rs17217772(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410107
GeneMSH2
is asnp
is mentioned by
dbSNPrs17217772
ebirs17217772
HLIrs17217772
Exacrs17217772
Varsomers17217772
Maprs17217772
PheGenIrs17217772
hapmaprs17217772
1000 genomesrs17217772
hgdprs17217772
ensemblrs17217772
gopubmedrs17217772
geneviewrs17217772
scholarrs17217772
googlers17217772
pharmgkbrs17217772
gwascentralrs17217772
openSNPrs17217772
23andMers17217772
23andMe allrs17217772
SNP Nexus

SNPshotrs17217772
SNPdbers17217772
MSV3drs17217772
GWAS Ctlgrs17217772
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 25134804OA-icon.png] 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,T;G,T)
Alt rs17217772(G,T;G,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 International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000030253.3, RCV000035361.7, RCV000144619.1, RCV000162398.1, RCV000076589.2,