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rs876661059

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661059(-;-)
Make rs876661059(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37020454
GeneMLH1
is asnp
is mentioned by
dbSNPrs876661059
ebirs876661059
HLIrs876661059
Exacrs876661059
Varsomers876661059
Maprs876661059
PheGenIrs876661059
hapmaprs876661059
1000 genomesrs876661059
hgdprs876661059
ensemblrs876661059
gopubmedrs876661059
geneviewrs876661059
scholarrs876661059
googlers876661059
pharmgkbrs876661059
gwascentralrs876661059
openSNPrs876661059
23andMers876661059
23andMe allrs876661059
SNP Nexus

SNPshotrs876661059
SNPdbers876661059
MSV3drs876661059
GWAS Ctlgrs876661059
Max Magnitude0
ClinVar
Risk rs876661059(;)
Alt rs876661059(;)
Reference rs876661059(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MLH1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.37061945delC
CLNSRC
CLNACC RCV000219234.1,