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rs63750305

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs63750305(-;-)
Make rs63750305(-;AT)
Make rs63750305(AT;AT)
ReferenceGRCh38 38.1/142
Chromosome3
Position37025726
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750305
ebirs63750305
HLIrs63750305
Exacrs63750305
Varsomers63750305
Maprs63750305
PheGenIrs63750305
hapmaprs63750305
1000 genomesrs63750305
hgdprs63750305
ensemblrs63750305
gopubmedrs63750305
geneviewrs63750305
scholarrs63750305
googlers63750305
pharmgkbrs63750305
gwascentralrs63750305
openSNPrs63750305
23andMers63750305
23andMe allrs63750305
SNP Nexus

SNPshotrs63750305
SNPdbers63750305
MSV3drs63750305
GWAS Ctlgrs63750305
Max Magnitude0
ClinVar
Risk rs63750305(AT;AT)
Alt rs63750305(AT;AT)
Reference rs63750305(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067217_37067218dupTA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075114.2,