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

rs730881829

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881829(-;-)
Make rs730881829(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47806247
GeneMSH6
is asnp
is mentioned by
dbSNPrs730881829
ebirs730881829
HLIrs730881829
Exacrs730881829
Varsomers730881829
Maprs730881829
PheGenIrs730881829
hapmaprs730881829
1000 genomesrs730881829
hgdprs730881829
ensemblrs730881829
gopubmedrs730881829
geneviewrs730881829
scholarrs730881829
googlers730881829
pharmgkbrs730881829
gwascentralrs730881829
openSNPrs730881829
23andMers730881829
23andMe allrs730881829
SNP Nexus

SNPshotrs730881829
SNPdbers730881829
MSV3drs730881829
GWAS Ctlgrs730881829
Max Magnitude0
ClinVar
Risk rs730881829(;)
Alt rs730881829(;)
Reference rs730881829(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033386delA
CLNSRC
CLNACC RCV000160745.1, RCV000205295.1,