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rs864622457

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864622457(C;G)
Make rs864622457(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37050559
GeneMLH1
is asnp
is mentioned by
dbSNPrs864622457
ebirs864622457
HLIrs864622457
Exacrs864622457
Varsomers864622457
Maprs864622457
PheGenIrs864622457
hapmaprs864622457
1000 genomesrs864622457
hgdprs864622457
ensemblrs864622457
gopubmedrs864622457
geneviewrs864622457
scholarrs864622457
googlers864622457
pharmgkbrs864622457
gwascentralrs864622457
openSNPrs864622457
23andMers864622457
23andMe allrs864622457
SNP Nexus

SNPshotrs864622457
SNPdbers864622457
MSV3drs864622457
GWAS Ctlgrs864622457
Max Magnitude0
ClinVar
Risk rs864622457(G;G)
Alt rs864622457(G;G)
Reference rs864622457(C;C)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37092050C>G
CLNSRC
CLNACC RCV000204293.1,