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rs63750906

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63750906(-;-)
Make rs63750906(-;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37004440
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750906
ebirs63750906
HLIrs63750906
Exacrs63750906
Varsomers63750906
Maprs63750906
PheGenIrs63750906
hapmaprs63750906
1000 genomesrs63750906
hgdprs63750906
ensemblrs63750906
gopubmedrs63750906
geneviewrs63750906
scholarrs63750906
googlers63750906
pharmgkbrs63750906
gwascentralrs63750906
openSNPrs63750906
23andMers63750906
23andMe allrs63750906
SNP Nexus

SNPshotrs63750906
SNPdbers63750906
MSV3drs63750906
GWAS Ctlgrs63750906
Max Magnitude0
ClinVar
Risk rs63750906(;)
Alt rs63750906(;)
Reference rs63750906(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37045931delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075661.2,