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rs63750319

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750319(-;-)
Make rs63750319(-;A)
Make rs63750319(A;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37020360
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750319
ebirs63750319
HLIrs63750319
Exacrs63750319
Varsomers63750319
Maprs63750319
PheGenIrs63750319
hapmaprs63750319
1000 genomesrs63750319
hgdprs63750319
ensemblrs63750319
gopubmedrs63750319
geneviewrs63750319
scholarrs63750319
googlers63750319
pharmgkbrs63750319
gwascentralrs63750319
openSNPrs63750319
23andMers63750319
23andMe allrs63750319
SNP Nexus

SNPshotrs63750319
SNPdbers63750319
MSV3drs63750319
GWAS Ctlgrs63750319
Max Magnitude0
ClinVar
Risk rs63750319(A;A)
Alt rs63750319(A;A)
Reference rs63750319(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061851dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075941.2,