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rs63750952

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63750952(A;G)
Make rs63750952(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996693
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750952
ebirs63750952
HLIrs63750952
Exacrs63750952
Varsomers63750952
Maprs63750952
PheGenIrs63750952
hapmaprs63750952
1000 genomesrs63750952
hgdprs63750952
ensemblrs63750952
gopubmedrs63750952
geneviewrs63750952
scholarrs63750952
googlers63750952
pharmgkbrs63750952
gwascentralrs63750952
openSNPrs63750952
23andMers63750952
23andMe allrs63750952
SNP Nexus

SNPshotrs63750952
SNPdbers63750952
MSV3drs63750952
GWAS Ctlgrs63750952
Max Magnitude0
ClinVar
Risk rs63750952(G;G)
Alt rs63750952(G;G)
Reference rs63750952(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome not specified Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN Lynch syndrome not specified Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37038184A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075426.3, RCV000160536.2, RCV000217492.1,