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rs63749874

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
(AAGA;AAGA) 0 common in clinvar
(I;I) 0
Make rs63749874(-;-)
Make rs63749874(-;AAGA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47799617
GeneMSH6
is asnp
is mentioned by
dbSNPrs63749874
ebirs63749874
HLIrs63749874
Exacrs63749874
Varsomers63749874
Maprs63749874
PheGenIrs63749874
hapmaprs63749874
1000 genomesrs63749874
hgdprs63749874
ensemblrs63749874
gopubmedrs63749874
geneviewrs63749874
scholarrs63749874
googlers63749874
pharmgkbrs63749874
gwascentralrs63749874
openSNPrs63749874
23andMers63749874
23andMe allrs63749874
SNP Nexus

SNPshotrs63749874
SNPdbers63749874
MSV3drs63749874
GWAS Ctlgrs63749874
Max Magnitude0
ClinVar
Risk rs63749874(;)
Alt rs63749874(;)
Reference rs63749874(AAAG;AAAG)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48026756_48026759delAAGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074674.2, RCV000115378.3,