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rs876659681

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs876659681(-;TT)
Make rs876659681(TT;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37048984
GeneMLH1
is asnp
is mentioned by
dbSNPrs876659681
dbSNP (classic)rs876659681
ClinGenrs876659681
ebirs876659681
HLIrs876659681
Exacrs876659681
Gnomadrs876659681
Varsomers876659681
LitVarrs876659681
Maprs876659681
PheGenIrs876659681
Biobankrs876659681
1000 genomesrs876659681
hgdprs876659681
ensemblrs876659681
geneviewrs876659681
scholarrs876659681
googlers876659681
pharmgkbrs876659681
gwascentralrs876659681
openSNPrs876659681
23andMers876659681
SNPshotrs876659681
SNPdbers876659681
MSV3drs876659681
GWAS Ctlgrs876659681
Max Magnitude0
ClinVar
Risk rs876659681(TT;TT)
Alt rs876659681(TT;TT)
Reference Rs876659681(-;-)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37090475_37090476insTT
CLNSRC
CLNACC RCV000221270.1,