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rs876661205

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661205(-;-)
Make rs876661205(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47799952
GeneMSH6
is asnp
is mentioned by
dbSNPrs876661205
ebirs876661205
HLIrs876661205
Exacrs876661205
Varsomers876661205
Maprs876661205
PheGenIrs876661205
hapmaprs876661205
1000 genomesrs876661205
hgdprs876661205
ensemblrs876661205
gopubmedrs876661205
geneviewrs876661205
scholarrs876661205
googlers876661205
pharmgkbrs876661205
gwascentralrs876661205
openSNPrs876661205
23andMers876661205
23andMe allrs876661205
SNP Nexus

SNPshotrs876661205
SNPdbers876661205
MSV3drs876661205
GWAS Ctlgrs876661205
Max Magnitude0
ClinVar
Risk rs876661205(;)
Alt rs876661205(;)
Reference rs876661205(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48027091delC
CLNSRC
CLNACC RCV000215322.1,