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rs796052949

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052949(-;-)
Make rs796052949(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position76163286
GeneSCARB2
is asnp
is mentioned by
dbSNPrs796052949
ebirs796052949
HLIrs796052949
Exacrs796052949
Varsomers796052949
Maprs796052949
PheGenIrs796052949
hapmaprs796052949
1000 genomesrs796052949
hgdprs796052949
ensemblrs796052949
gopubmedrs796052949
geneviewrs796052949
scholarrs796052949
googlers796052949
pharmgkbrs796052949
gwascentralrs796052949
openSNPrs796052949
23andMers796052949
23andMe allrs796052949
SNP Nexus

SNPshotrs796052949
SNPdbers796052949
MSV3drs796052949
GWAS Ctlgrs796052949
Max Magnitude0
ClinVar
Risk rs796052949(;)
Alt rs796052949(;)
Reference rs796052949(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCARB2
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.77084439delC
CLNSRC
CLNACC RCV000188811.1,