Have questions? Visit https://www.reddit.com/r/SNPedia

rs730881825

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881825(-;-)
Make rs730881825(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799825
GeneMSH6
is asnp
is mentioned by
dbSNPrs730881825
ebirs730881825
HLIrs730881825
Exacrs730881825
Varsomers730881825
Maprs730881825
PheGenIrs730881825
hapmaprs730881825
1000 genomesrs730881825
hgdprs730881825
ensemblrs730881825
gopubmedrs730881825
geneviewrs730881825
scholarrs730881825
googlers730881825
pharmgkbrs730881825
gwascentralrs730881825
openSNPrs730881825
23andMers730881825
23andMe allrs730881825
SNP Nexus

SNPshotrs730881825
SNPdbers730881825
MSV3drs730881825
GWAS Ctlgrs730881825
Max Magnitude0
ClinVar
Risk rs730881825(;)
Alt rs730881825(;)
Reference rs730881825(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48026964delC
CLNSRC
CLNACC RCV000160741.1,