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rs864622435

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864622435(G;T)
Make rs864622435(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47799370
GeneMSH6
is asnp
is mentioned by
dbSNPrs864622435
ebirs864622435
HLIrs864622435
Exacrs864622435
Varsomers864622435
Maprs864622435
PheGenIrs864622435
hapmaprs864622435
1000 genomesrs864622435
hgdprs864622435
ensemblrs864622435
gopubmedrs864622435
geneviewrs864622435
scholarrs864622435
googlers864622435
pharmgkbrs864622435
gwascentralrs864622435
openSNPrs864622435
23andMers864622435
23andMe allrs864622435
SNP Nexus

SNPshotrs864622435
SNPdbers864622435
MSV3drs864622435
GWAS Ctlgrs864622435
Max Magnitude0
ClinVar
Risk rs864622435(T;T)
Alt rs864622435(T;T)
Reference rs864622435(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026509G>T
CLNSRC
CLNACC RCV000206852.2,