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rs876660458

From SNPedia

Orientationplus
Geno Mag Summary
(GTCTGGT;GTCTGGT) 0 common in clinvar
Make rs876660458(-;-)
Make rs876660458(-;GTCTGGT)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37017509
GeneMLH1
is asnp
is mentioned by
dbSNPrs876660458
ebirs876660458
HLIrs876660458
Exacrs876660458
Varsomers876660458
Maprs876660458
PheGenIrs876660458
hapmaprs876660458
1000 genomesrs876660458
hgdprs876660458
ensemblrs876660458
gopubmedrs876660458
geneviewrs876660458
scholarrs876660458
googlers876660458
pharmgkbrs876660458
gwascentralrs876660458
openSNPrs876660458
23andMers876660458
23andMe allrs876660458
SNP Nexus

SNPshotrs876660458
SNPdbers876660458
MSV3drs876660458
GWAS Ctlgrs876660458
Max Magnitude0
ClinVar
Risk rs876660458(;)
Alt rs876660458(;)
Reference rs876660458(GTCTGGT;GTCTGGT)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37059000_37059006delGTCTGGT
CLNSRC
CLNACC RCV000213425.1,