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rs63750760

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750760(C;T)
Make rs63750760(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025751
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750760
dbSNP (classic)rs63750760
ClinGenrs63750760
ebirs63750760
HLIrs63750760
Exacrs63750760
Gnomadrs63750760
Varsomers63750760
LitVarrs63750760
Maprs63750760
PheGenIrs63750760
Biobankrs63750760
1000 genomesrs63750760
hgdprs63750760
ensemblrs63750760
geneviewrs63750760
scholarrs63750760
googlers63750760
pharmgkbrs63750760
gwascentralrs63750760
openSNPrs63750760
23andMers63750760
SNPshotrs63750760
SNPdbers63750760
MSV3drs63750760
GWAS Ctlgrs63750760
Max Magnitude0
ClinVar
Risk rs63750760(T;T)
Alt rs63750760(T;T)
Reference Rs63750760(C;C)
Significance Other
Disease Lynch syndrome not specified Hereditary cancer-predisposing syndrome Lynch syndrome II Lynch syndrome I
Variation info
Gene MLH1
CLNDBN Lynch syndrome not specified Hereditary cancer-predisposing syndrome Lynch syndrome II Lynch syndrome I
Reversed 0
HGVS NC_000003.11:g.37067242C>T
CLNSRC UniProtKB (protein)
CLNACC RCV000075124.2, RCV000202088.1, RCV000217569.2, RCV000490290.1, RCV000490570.1,