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

rs763978082

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs763978082(-;-)
Make rs763978082(-;A)
Make rs763978082(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800761
GeneMSH6
is asnp
is mentioned by
dbSNPrs763978082
ebirs763978082
HLIrs763978082
Exacrs763978082
Varsomers763978082
Maprs763978082
PheGenIrs763978082
hapmaprs763978082
1000 genomesrs763978082
hgdprs763978082
ensemblrs763978082
gopubmedrs763978082
geneviewrs763978082
scholarrs763978082
googlers763978082
pharmgkbrs763978082
gwascentralrs763978082
openSNPrs763978082
23andMers763978082
23andMe allrs763978082
SNP Nexus

SNPshotrs763978082
SNPdbers763978082
MSV3drs763978082
GWAS Ctlgrs763978082
Max Magnitude0
ClinVar
Risk rs763978082(A;A)
Alt rs763978082(A;A)
Reference rs763978082(;)
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.48027901dupA
CLNSRC
CLNACC RCV000131134.2, RCV000218611.1,