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rs63750150

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
(I;I) 0
Make rs63750150(-;-)
Make rs63750150(-;AT)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047618
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750150
ebirs63750150
HLIrs63750150
Exacrs63750150
Varsomers63750150
Maprs63750150
PheGenIrs63750150
hapmaprs63750150
1000 genomesrs63750150
hgdprs63750150
ensemblrs63750150
gopubmedrs63750150
geneviewrs63750150
scholarrs63750150
googlers63750150
pharmgkbrs63750150
gwascentralrs63750150
openSNPrs63750150
23andMers63750150
23andMe allrs63750150
SNP Nexus

SNPshotrs63750150
SNPdbers63750150
MSV3drs63750150
GWAS Ctlgrs63750150
Max Magnitude0
ClinVar
Risk rs63750150(;)
Alt rs63750150(;)
Reference rs63750150(AT;AT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089109_37089110delAT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075376.2,