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rs63750971

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
(CA;CA) 0 common in clinvar
(I;I) 0
Make rs63750971(-;-)
Make rs63750971(-;CA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37050536
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750971
ebirs63750971
HLIrs63750971
Exacrs63750971
Varsomers63750971
Maprs63750971
PheGenIrs63750971
hapmaprs63750971
1000 genomesrs63750971
hgdprs63750971
ensemblrs63750971
gopubmedrs63750971
geneviewrs63750971
scholarrs63750971
googlers63750971
pharmgkbrs63750971
gwascentralrs63750971
openSNPrs63750971
23andMers63750971
23andMe allrs63750971
SNP Nexus

SNPshotrs63750971
SNPdbers63750971
MSV3drs63750971
GWAS Ctlgrs63750971
Max Magnitude0
ClinVar
Risk rs63750971(;)
Alt rs63750971(;)
Reference rs63750971(AC;AC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37092027_37092028delCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075558.2,