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rs63750282

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63750282(-;-)
Make rs63750282(-;A)
Make rs63750282(A;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048914
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750282
ebirs63750282
HLIrs63750282
Exacrs63750282
Varsomers63750282
Maprs63750282
PheGenIrs63750282
hapmaprs63750282
1000 genomesrs63750282
hgdprs63750282
ensemblrs63750282
gopubmedrs63750282
geneviewrs63750282
scholarrs63750282
googlers63750282
pharmgkbrs63750282
gwascentralrs63750282
openSNPrs63750282
23andMers63750282
23andMe allrs63750282
SNP Nexus

SNPshotrs63750282
SNPdbers63750282
MSV3drs63750282
GWAS Ctlgrs63750282
Max Magnitude0
ClinVar
Risk rs63750282(A;A)
Alt rs63750282(A;A)
Reference rs63750282(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090405dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075478.2,