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rs796065037

From SNPedia

Orientationminus
Geno Mag Summary
(GAT;GAT) 0 common in clinvar
Make rs796065037(-;-)
Make rs796065037(-;GAT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position15536505
GeneNBAS
is asnp
is mentioned by
dbSNPrs796065037
ebirs796065037
HLIrs796065037
Exacrs796065037
Varsomers796065037
Maprs796065037
PheGenIrs796065037
hapmaprs796065037
1000 genomesrs796065037
hgdprs796065037
ensemblrs796065037
gopubmedrs796065037
geneviewrs796065037
scholarrs796065037
googlers796065037
pharmgkbrs796065037
gwascentralrs796065037
openSNPrs796065037
23andMers796065037
23andMe allrs796065037
SNP Nexus

SNPshotrs796065037
SNPdbers796065037
MSV3drs796065037
GWAS Ctlgrs796065037
Max Magnitude0
ClinVar
Risk rs796065037(;)
Alt rs796065037(;)
Reference rs796065037(GAT;GAT)
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.15676629_15676631delATC
CLNSRC OMIM Allelic Variant
CLNACC RCV000186577.2,