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

rs63750303

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750303(A;A)
Make rs63750303(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37014485
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750303
ebirs63750303
HLIrs63750303
Exacrs63750303
Varsomers63750303
Maprs63750303
PheGenIrs63750303
hapmaprs63750303
1000 genomesrs63750303
hgdprs63750303
ensemblrs63750303
gopubmedrs63750303
geneviewrs63750303
scholarrs63750303
googlers63750303
pharmgkbrs63750303
gwascentralrs63750303
openSNPrs63750303
23andMers63750303
23andMe allrs63750303
SNP Nexus

SNPshotrs63750303
SNPdbers63750303
MSV3drs63750303
GWAS Ctlgrs63750303
Max Magnitude0
ClinVar
Risk rs63750303(A,T;A,T)
Alt rs63750303(A,T;A,T)
Reference rs63750303(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37055976G>A; NC_000003.11:g.37055976G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075830.2, RCV000075831.2,