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rs63751595

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751595(A;A)
Make rs63751595(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37004474
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751595
ebirs63751595
HLIrs63751595
Exacrs63751595
Varsomers63751595
Maprs63751595
PheGenIrs63751595
hapmaprs63751595
1000 genomesrs63751595
hgdprs63751595
ensemblrs63751595
gopubmedrs63751595
geneviewrs63751595
scholarrs63751595
googlers63751595
pharmgkbrs63751595
gwascentralrs63751595
openSNPrs63751595
23andMers63751595
23andMe allrs63751595
SNP Nexus

SNPshotrs63751595
SNPdbers63751595
MSV3drs63751595
GWAS Ctlgrs63751595
Max Magnitude0
ClinVar
Risk rs63751595(A,T;A,T)
Alt rs63751595(A,T;A,T)
Reference rs63751595(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000003.11:g.37045965G>A; NC_000003.11:g.37045965G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075682.2, RCV000221216.1, RCV000160521.1,