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

rs876661222

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876661222(-;-)
Make rs876661222(-;ATTA)
Make rs876661222(ATTA;ATTA)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47806313
GeneMSH6
is asnp
is mentioned by
dbSNPrs876661222
ebirs876661222
HLIrs876661222
Exacrs876661222
Varsomers876661222
Maprs876661222
PheGenIrs876661222
hapmaprs876661222
1000 genomesrs876661222
hgdprs876661222
ensemblrs876661222
gopubmedrs876661222
geneviewrs876661222
scholarrs876661222
googlers876661222
pharmgkbrs876661222
gwascentralrs876661222
openSNPrs876661222
23andMers876661222
23andMe allrs876661222
SNP Nexus

SNPshotrs876661222
SNPdbers876661222
MSV3drs876661222
GWAS Ctlgrs876661222
Max Magnitude0
ClinVar
Risk rs876661222(ATTA;ATTA)
Alt rs876661222(ATTA;ATTA)
Reference rs876661222(;)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48033449_48033452dupATTA
CLNSRC
CLNACC RCV000216513.1,