Have questions? Visit https://www.reddit.com/r/SNPedia

rs63751194

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751194(C;T)
Make rs63751194(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017508
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751194
ebirs63751194
HLIrs63751194
Exacrs63751194
Varsomers63751194
Maprs63751194
PheGenIrs63751194
hapmaprs63751194
1000 genomesrs63751194
hgdprs63751194
ensemblrs63751194
gopubmedrs63751194
geneviewrs63751194
scholarrs63751194
googlers63751194
pharmgkbrs63751194
gwascentralrs63751194
openSNPrs63751194
23andMers63751194
23andMe allrs63751194
SNP Nexus

SNPshotrs63751194
SNPdbers63751194
MSV3drs63751194
GWAS Ctlgrs63751194
Max Magnitude0
ClinVar
Risk rs63751194(A,T;A,T)
Alt rs63751194(A,T;A,T)
Reference rs63751194(C;C)
Significance Other
Disease Lynch syndrome not provided Lynch syndrome II Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided Lynch syndrome II Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37058999C>A; NC_000003.11:g.37058999C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours OMIM Allelic Variant
CLNACC RCV000075871.2, RCV000202126.1, RCV000022502.23, RCV000034802.2, RCV000075872.2, RCV000220712.1,