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rs730881826

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881826(-;-)
Make rs730881826(-;T)
Make rs730881826(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47798685
GeneMSH6
is asnp
is mentioned by
dbSNPrs730881826
ebirs730881826
HLIrs730881826
Exacrs730881826
Varsomers730881826
Maprs730881826
PheGenIrs730881826
hapmaprs730881826
1000 genomesrs730881826
hgdprs730881826
ensemblrs730881826
gopubmedrs730881826
geneviewrs730881826
scholarrs730881826
googlers730881826
pharmgkbrs730881826
gwascentralrs730881826
openSNPrs730881826
23andMers730881826
23andMe allrs730881826
SNP Nexus

SNPshotrs730881826
SNPdbers730881826
MSV3drs730881826
GWAS Ctlgrs730881826
Max Magnitude0
ClinVar
Risk rs730881826(T;T)
Alt rs730881826(T;T)
Reference rs730881826(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48025824_48025825insT
CLNSRC
CLNACC RCV000160742.1,