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rs727504146

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504146(-;-)
Make rs727504146(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position107957901
GeneSEC63
is asnp
is mentioned by
dbSNPrs727504146
ebirs727504146
HLIrs727504146
Exacrs727504146
Varsomers727504146
Maprs727504146
PheGenIrs727504146
hapmaprs727504146
1000 genomesrs727504146
hgdprs727504146
ensemblrs727504146
gopubmedrs727504146
geneviewrs727504146
scholarrs727504146
googlers727504146
pharmgkbrs727504146
gwascentralrs727504146
openSNPrs727504146
23andMers727504146
23andMe allrs727504146
SNP Nexus

SNPshotrs727504146
SNPdbers727504146
MSV3drs727504146
GWAS Ctlgrs727504146
Max Magnitude0
ClinVar
Risk rs727504146(;)
Alt rs727504146(;)
Reference rs727504146(C;C)
Significance Pathogenic
Disease not provided Congenital cystic disease of liver
Variation info
Gene SEC63
CLNDBN not provided Congenital cystic disease of liver
Reversed 1
HGVS NC_000006.11:g.108279105delG
CLNSRC
CLNACC RCV000153932.2, RCV000173417.1,