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rs796052121

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052121(C;C)
Make rs796052121(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position15394320
GeneNBAS
is asnp
is mentioned by
dbSNPrs796052121
ebirs796052121
HLIrs796052121
Exacrs796052121
Varsomers796052121
Maprs796052121
PheGenIrs796052121
hapmaprs796052121
1000 genomesrs796052121
hgdprs796052121
ensemblrs796052121
gopubmedrs796052121
geneviewrs796052121
scholarrs796052121
googlers796052121
pharmgkbrs796052121
gwascentralrs796052121
openSNPrs796052121
23andMers796052121
23andMe allrs796052121
SNP Nexus

SNPshotrs796052121
SNPdbers796052121
MSV3drs796052121
GWAS Ctlgrs796052121
Max Magnitude0
ClinVar
Risk rs796052121(C;C)
Alt rs796052121(C;C)
Reference rs796052121(T;T)
Significance Pathogenic
Disease Infantile liver failure syndrome 2
Variation info
Gene NBAS
CLNDBN Infantile liver failure syndrome 2
Reversed 1
HGVS NC_000002.11:g.15534444A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000186581.2,