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rs730881733

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs730881733(-;-)
Make rs730881733(-;AA)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36996657
GeneMLH1
is asnp
is mentioned by
dbSNPrs730881733
ebirs730881733
HLIrs730881733
Exacrs730881733
Varsomers730881733
Maprs730881733
PheGenIrs730881733
hapmaprs730881733
1000 genomesrs730881733
hgdprs730881733
ensemblrs730881733
gopubmedrs730881733
geneviewrs730881733
scholarrs730881733
googlers730881733
pharmgkbrs730881733
gwascentralrs730881733
openSNPrs730881733
23andMers730881733
23andMe allrs730881733
SNP Nexus

SNPshotrs730881733
SNPdbers730881733
MSV3drs730881733
GWAS Ctlgrs730881733
Max Magnitude0
ClinVar
Risk rs730881733(;)
Alt rs730881733(;)
Reference rs730881733(AA;AA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37038148_37038149delAA
CLNSRC
CLNACC RCV000160515.1,