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rs63750036

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs63750036(-;-)
Make rs63750036(-;GG)
ReferenceGRCh38 38.1/141
Chromosome3
Position37040247
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750036
ebirs63750036
HLIrs63750036
Exacrs63750036
Varsomers63750036
Maprs63750036
PheGenIrs63750036
hapmaprs63750036
1000 genomesrs63750036
hgdprs63750036
ensemblrs63750036
gopubmedrs63750036
geneviewrs63750036
scholarrs63750036
googlers63750036
pharmgkbrs63750036
gwascentralrs63750036
openSNPrs63750036
23andMers63750036
23andMe allrs63750036
SNP Nexus

SNPshotrs63750036
SNPdbers63750036
MSV3drs63750036
GWAS Ctlgrs63750036
Max Magnitude0
ClinVar
Risk rs63750036(;)
Alt rs63750036(;)
Reference rs63750036(GG;GG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081738_37081739delGG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075281.2,