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

rs587781398

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs587781398(-;-)
Make rs587781398(-;AA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799617
GeneMSH6
is asnp
is mentioned by
dbSNPrs587781398
ebirs587781398
HLIrs587781398
Exacrs587781398
Varsomers587781398
Maprs587781398
PheGenIrs587781398
hapmaprs587781398
1000 genomesrs587781398
hgdprs587781398
ensemblrs587781398
gopubmedrs587781398
geneviewrs587781398
scholarrs587781398
googlers587781398
pharmgkbrs587781398
gwascentralrs587781398
openSNPrs587781398
23andMers587781398
23andMe allrs587781398
SNP Nexus

SNPshotrs587781398
SNPdbers587781398
MSV3drs587781398
GWAS Ctlgrs587781398
Max Magnitude0
ClinVar
Risk rs587781398(;)
Alt rs587781398(;)
Reference rs587781398(AA;AA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48026756_48026757delAA
CLNSRC
CLNACC RCV000129244.2, RCV000202281.1,