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rs786202037

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786202037(-;-)
Make rs786202037(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47408440
GeneMSH2
is asnp
is mentioned by
dbSNPrs786202037
ebirs786202037
HLIrs786202037
Exacrs786202037
Varsomers786202037
Maprs786202037
PheGenIrs786202037
hapmaprs786202037
1000 genomesrs786202037
hgdprs786202037
ensemblrs786202037
gopubmedrs786202037
geneviewrs786202037
scholarrs786202037
googlers786202037
pharmgkbrs786202037
gwascentralrs786202037
openSNPrs786202037
23andMers786202037
23andMe allrs786202037
SNP Nexus

SNPshotrs786202037
SNPdbers786202037
MSV3drs786202037
GWAS Ctlgrs786202037
Max Magnitude0
ClinVar
Risk rs786202037(;)
Alt rs786202037(;)
Reference rs786202037(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47635579delA
CLNSRC
CLNACC RCV000164646.1,