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rs200053119

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200053119(A;A)
Make rs200053119(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position76181016
GeneSCARB2
is asnp
is mentioned by
dbSNPrs200053119
ebirs200053119
HLIrs200053119
Exacrs200053119
Varsomers200053119
Maprs200053119
PheGenIrs200053119
hapmaprs200053119
1000 genomesrs200053119
hgdprs200053119
ensemblrs200053119
gopubmedrs200053119
geneviewrs200053119
scholarrs200053119
googlers200053119
pharmgkbrs200053119
gwascentralrs200053119
openSNPrs200053119
23andMers200053119
23andMe allrs200053119
SNP Nexus

SNPshotrs200053119
SNPdbers200053119
MSV3drs200053119
GWAS Ctlgrs200053119
Max Magnitude0
ClinVar
Risk rs200053119(A;A)
Alt rs200053119(A;A)
Reference rs200053119(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCARB2
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.77102169G>A
CLNSRC
CLNACC RCV000188795.1,