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rs869312977

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312977(A;A)
Make rs869312977(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position107921796
GeneSEC63
is asnp
is mentioned by
dbSNPrs869312977
ebirs869312977
HLIrs869312977
Exacrs869312977
Varsomers869312977
Maprs869312977
PheGenIrs869312977
hapmaprs869312977
1000 genomesrs869312977
hgdprs869312977
ensemblrs869312977
gopubmedrs869312977
geneviewrs869312977
scholarrs869312977
googlers869312977
pharmgkbrs869312977
gwascentralrs869312977
openSNPrs869312977
23andMers869312977
23andMe allrs869312977
SNP Nexus

SNPshotrs869312977
SNPdbers869312977
MSV3drs869312977
GWAS Ctlgrs869312977
Max Magnitude0
ClinVar
Risk rs869312977(A;A)
Alt rs869312977(A;A)
Reference rs869312977(G;G)
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.108243000C>T
CLNSRC
CLNACC RCV000210666.1,