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rs797044920

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044920(C;C)
Make rs797044920(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position92719056
GeneBICD2
is asnp
is mentioned by
dbSNPrs797044920
ebirs797044920
HLIrs797044920
Exacrs797044920
Varsomers797044920
Maprs797044920
PheGenIrs797044920
hapmaprs797044920
1000 genomesrs797044920
hgdprs797044920
ensemblrs797044920
gopubmedrs797044920
geneviewrs797044920
scholarrs797044920
googlers797044920
pharmgkbrs797044920
gwascentralrs797044920
openSNPrs797044920
23andMers797044920
23andMe allrs797044920
SNP Nexus

SNPshotrs797044920
SNPdbers797044920
MSV3drs797044920
GWAS Ctlgrs797044920
Max Magnitude0
ClinVar
Risk rs797044920(C;C)
Alt rs797044920(C;C)
Reference rs797044920(T;T)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene BICD2
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000009.11:g.95481338A>G
CLNSRC
CLNACC RCV000190756.1,