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

rs864622153

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864622153(A;A)
Make rs864622153(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47799674
GeneMSH6
is asnp
is mentioned by
dbSNPrs864622153
ebirs864622153
HLIrs864622153
Exacrs864622153
Varsomers864622153
Maprs864622153
PheGenIrs864622153
hapmaprs864622153
1000 genomesrs864622153
hgdprs864622153
ensemblrs864622153
gopubmedrs864622153
geneviewrs864622153
scholarrs864622153
googlers864622153
pharmgkbrs864622153
gwascentralrs864622153
openSNPrs864622153
23andMers864622153
23andMe allrs864622153
SNP Nexus

SNPshotrs864622153
SNPdbers864622153
MSV3drs864622153
GWAS Ctlgrs864622153
Max Magnitude0
ClinVar
Risk rs864622153(A;A)
Alt rs864622153(A;A)
Reference rs864622153(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026813C>A
CLNSRC
CLNACC RCV000204908.1,