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rs797044656

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044656(-;A)
Make rs797044656(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position107893550
GeneSEC63
is asnp
is mentioned by
dbSNPrs797044656
ClinGenrs797044656
ebirs797044656
HLIrs797044656
Exacrs797044656
Varsomers797044656
Maprs797044656
PheGenIrs797044656
hapmaprs797044656
1000 genomesrs797044656
hgdprs797044656
ensemblrs797044656
gopubmedrs797044656
geneviewrs797044656
scholarrs797044656
googlers797044656
pharmgkbrs797044656
gwascentralrs797044656
openSNPrs797044656
23andMers797044656
23andMe allrs797044656
SNP Nexus

SNPshotrs797044656
SNPdbers797044656
MSV3drs797044656
GWAS Ctlgrs797044656
Max Magnitude0
ClinVar
Risk rs797044656(A;A)
Alt rs797044656(A;A)
Reference Rs797044656(-;-)
Significance Pathogenic
Disease Congenital cystic disease of liver
Variation info
Gene SEC63
CLNDBN Congenital cystic disease of liver
Reversed 1
HGVS NC_000006.11:g.108214755dupT
CLNSRC
CLNACC RCV000175067.1,