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

rs63750131

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CG;CG) 0 common in clinvar
Make rs63750131(-;-)
Make rs63750131(-;CG)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048595
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750131
ebirs63750131
HLIrs63750131
Exacrs63750131
Varsomers63750131
Maprs63750131
PheGenIrs63750131
hapmaprs63750131
1000 genomesrs63750131
hgdprs63750131
ensemblrs63750131
gopubmedrs63750131
geneviewrs63750131
scholarrs63750131
googlers63750131
pharmgkbrs63750131
gwascentralrs63750131
openSNPrs63750131
23andMers63750131
23andMe allrs63750131
SNP Nexus

SNPshotrs63750131
SNPdbers63750131
MSV3drs63750131
GWAS Ctlgrs63750131
Max Magnitude0
ClinVar
Risk rs63750131(;)
Alt rs63750131(;)
Reference rs63750131(CG;CG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090086_37090087delCG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075445.2,