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rs876661159

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661159(-;-)
Make rs876661159(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37004441
GeneMLH1
is asnp
is mentioned by
dbSNPrs876661159
ebirs876661159
HLIrs876661159
Exacrs876661159
Varsomers876661159
Maprs876661159
PheGenIrs876661159
hapmaprs876661159
1000 genomesrs876661159
hgdprs876661159
ensemblrs876661159
gopubmedrs876661159
geneviewrs876661159
scholarrs876661159
googlers876661159
pharmgkbrs876661159
gwascentralrs876661159
openSNPrs876661159
23andMers876661159
23andMe allrs876661159
SNP Nexus

SNPshotrs876661159
SNPdbers876661159
MSV3drs876661159
GWAS Ctlgrs876661159
Max Magnitude0
ClinVar
Risk rs876661159(;)
Alt rs876661159(;)
Reference rs876661159(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MLH1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.37045932delC
CLNSRC
CLNACC RCV000223327.1,