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rs876658923

From SNPedia

Orientationplus
Geno Mag Summary
(GTGAACC;GTGAACC) 0 common in clinvar
Make rs876658923(-;-)
Make rs876658923(-;TGAACCG)
Make rs876658923(TGAACCG;TGAACCG)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position36993594
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs876658923
ebirs876658923
HLIrs876658923
Exacrs876658923
Varsomers876658923
Maprs876658923
PheGenIrs876658923
hapmaprs876658923
1000 genomesrs876658923
hgdprs876658923
ensemblrs876658923
gopubmedrs876658923
geneviewrs876658923
scholarrs876658923
googlers876658923
pharmgkbrs876658923
gwascentralrs876658923
openSNPrs876658923
23andMers876658923
23andMe allrs876658923
SNP Nexus

SNPshotrs876658923
SNPdbers876658923
MSV3drs876658923
GWAS Ctlgrs876658923
Max Magnitude0
ClinVar
Risk rs876658923(;)
Alt rs876658923(;)
Reference rs876658923(GTGAACC;GTGAACC)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37035085_37035091delTGAACCG
CLNSRC
CLNACC RCV000219515.1,