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rs368196005

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs368196005(A;C)
Make rs368196005(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position15417582
GeneNBAS
is asnp
is mentioned by
dbSNPrs368196005
ebirs368196005
HLIrs368196005
Exacrs368196005
Varsomers368196005
Maprs368196005
PheGenIrs368196005
hapmaprs368196005
1000 genomesrs368196005
hgdprs368196005
ensemblrs368196005
gopubmedrs368196005
geneviewrs368196005
scholarrs368196005
googlers368196005
pharmgkbrs368196005
gwascentralrs368196005
openSNPrs368196005
23andMers368196005
23andMe allrs368196005
SNP Nexus

SNPshotrs368196005
SNPdbers368196005
MSV3drs368196005
GWAS Ctlgrs368196005
Max Magnitude0
ClinVar
Risk rs368196005(C;C)
Alt rs368196005(C;C)
Reference rs368196005(A;A)
Significance Pathogenic
Disease Infantile liver failure syndrome 2
Variation info
Gene NBAS
CLNDBN Infantile liver failure syndrome 2
Reversed 0
HGVS NC_000002.11:g.15557706A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000186579.2,