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

rs786203331

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786203331(-;-)
Make rs786203331(-;AGTA)
Make rs786203331(AGTA;AGTA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47805626
GeneMSH6
is asnp
is mentioned by
dbSNPrs786203331
ebirs786203331
HLIrs786203331
Exacrs786203331
Varsomers786203331
Maprs786203331
PheGenIrs786203331
hapmaprs786203331
1000 genomesrs786203331
hgdprs786203331
ensemblrs786203331
gopubmedrs786203331
geneviewrs786203331
scholarrs786203331
googlers786203331
pharmgkbrs786203331
gwascentralrs786203331
openSNPrs786203331
23andMers786203331
23andMe allrs786203331
SNP Nexus

SNPshotrs786203331
SNPdbers786203331
MSV3drs786203331
GWAS Ctlgrs786203331
Max Magnitude0
ClinVar
Risk rs786203331(AAGT;AAGT)
Alt rs786203331(AAGT;AAGT)
Reference rs786203331(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48032762_48032765dupAGTA
CLNSRC
CLNACC RCV000166596.1,