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rs587776701

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776701(-;-)
Make rs587776701(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position80675103
GeneMSH3
is asnp
is mentioned by
dbSNPrs587776701
dbSNP (old)rs587776701
ClinGenrs587776701
ebirs587776701
HLIrs587776701
Exacrs587776701
Gnomadrs587776701
Varsomers587776701
Maprs587776701
PheGenIrs587776701
Biobankrs587776701
1000 genomesrs587776701
hgdprs587776701
ensemblrs587776701
gopubmedrs587776701
geneviewrs587776701
scholarrs587776701
googlers587776701
pharmgkbrs587776701
gwascentralrs587776701
openSNPrs587776701
23andMers587776701
23andMe allrs587776701
SNP Nexus

SNPshotrs587776701
SNPdbers587776701
MSV3drs587776701
GWAS Ctlgrs587776701
Max Magnitude0
ClinVar
Risk rs587776701(-;-)
Alt rs587776701(-;-)
Reference Rs587776701(A;A)
Significance Pathogenic
Disease Familial adenomatous polyposis 4 Endometrial carcinoma
Variation info
Gene MSH3
CLNDBN Familial adenomatous polyposis 4 Endometrial carcinoma
Reversed 0
HGVS NC_000005.9:g.79970922delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000009277.6, RCV000240050.1,