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rs63751665

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751665(G;T)
Make rs63751665(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37001053
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751665
ebirs63751665
HLIrs63751665
Exacrs63751665
Varsomers63751665
Maprs63751665
PheGenIrs63751665
hapmaprs63751665
1000 genomesrs63751665
hgdprs63751665
ensemblrs63751665
gopubmedrs63751665
geneviewrs63751665
scholarrs63751665
googlers63751665
pharmgkbrs63751665
gwascentralrs63751665
openSNPrs63751665
23andMers63751665
23andMe allrs63751665
SNP Nexus

SNPshotrs63751665
SNPdbers63751665
MSV3drs63751665
GWAS Ctlgrs63751665
Max Magnitude0
ClinVar
Risk rs63751665(A,C,T;A,C,T)
Alt rs63751665(A,C,T;A,C,T)
Reference rs63751665(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37042544G>A; NC_000003.11:g.37042544G>C; NC_000003.11:g.37042544G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000215920.1, RCV000075636.2, RCV000075637.2, RCV000115480.3, RCV000216647.1,