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

rs786204252

From SNPedia

Orientationplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs786204252(-;-)
Make rs786204252(-;TT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47799090
GeneMSH6
is asnp
is mentioned by
dbSNPrs786204252
ebirs786204252
HLIrs786204252
Exacrs786204252
Varsomers786204252
Maprs786204252
PheGenIrs786204252
hapmaprs786204252
1000 genomesrs786204252
hgdprs786204252
ensemblrs786204252
gopubmedrs786204252
geneviewrs786204252
scholarrs786204252
googlers786204252
pharmgkbrs786204252
gwascentralrs786204252
openSNPrs786204252
23andMers786204252
23andMe allrs786204252
SNP Nexus

SNPshotrs786204252
SNPdbers786204252
MSV3drs786204252
GWAS Ctlgrs786204252
Max Magnitude0
ClinVar
Risk rs786204252(;)
Alt rs786204252(;)
Reference rs786204252(TT;TT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026230_48026231delTT
CLNSRC
CLNACC RCV000168455.1,