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rs63750005

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750005(C;T)
Make rs63750005(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37000992
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750005
ebirs63750005
HLIrs63750005
Exacrs63750005
Varsomers63750005
Maprs63750005
PheGenIrs63750005
hapmaprs63750005
1000 genomesrs63750005
hgdprs63750005
ensemblrs63750005
gopubmedrs63750005
geneviewrs63750005
scholarrs63750005
googlers63750005
pharmgkbrs63750005
gwascentralrs63750005
openSNPrs63750005
23andMers63750005
23andMe allrs63750005
SNP Nexus

SNPshotrs63750005
SNPdbers63750005
MSV3drs63750005
GWAS Ctlgrs63750005
Max Magnitude0
ClinVar
Risk rs63750005(T;T)
Alt rs63750005(T;T)
Reference rs63750005(C;C)
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.37042483C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075604.2, RCV000222555.1,