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rs63751715

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751715(C;C)
Make rs63751715(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37020463
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751715
ebirs63751715
HLIrs63751715
Exacrs63751715
Varsomers63751715
Maprs63751715
PheGenIrs63751715
hapmaprs63751715
1000 genomesrs63751715
hgdprs63751715
ensemblrs63751715
gopubmedrs63751715
geneviewrs63751715
scholarrs63751715
googlers63751715
pharmgkbrs63751715
gwascentralrs63751715
openSNPrs63751715
23andMers63751715
23andMe allrs63751715
SNP Nexus

SNPshotrs63751715
SNPdbers63751715
MSV3drs63751715
GWAS Ctlgrs63751715
Max Magnitude0
ClinVar
Risk rs63751715(A,C,T;A,C,T)
Alt rs63751715(A,C,T;A,C,T)
Reference rs63751715(G;G)
Significance Pathogenic
Disease Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37061954G>A; NC_000003.11:g.37061954G>C; NC_000003.11:g.37061954G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075085.2, RCV000214854.1, RCV000075086.2, RCV000075087.2,