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rs370970617

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs370970617(C;T)
Make rs370970617(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47463125
GeneMSH2
is asnp
is mentioned by
dbSNPrs370970617
ebirs370970617
HLIrs370970617
Exacrs370970617
Varsomers370970617
Maprs370970617
PheGenIrs370970617
hapmaprs370970617
1000 genomesrs370970617
hgdprs370970617
ensemblrs370970617
gopubmedrs370970617
geneviewrs370970617
scholarrs370970617
googlers370970617
pharmgkbrs370970617
gwascentralrs370970617
openSNPrs370970617
23andMers370970617
23andMe allrs370970617
SNP Nexus

SNPshotrs370970617
SNPdbers370970617
MSV3drs370970617
GWAS Ctlgrs370970617
Max Magnitude0
ClinVar
Risk rs370970617(T;T)
Alt rs370970617(T;T)
Reference rs370970617(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47690264C>G
CLNSRC
CLNACC RCV000202035.1,