Have questions? Visit https://www.reddit.com/r/SNPedia

rs149688478

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149688478(A;A)
Make rs149688478(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position122947489
GeneSPATA5
is asnp
is mentioned by
dbSNPrs149688478
ebirs149688478
HLIrs149688478
Exacrs149688478
Varsomers149688478
Maprs149688478
PheGenIrs149688478
hapmaprs149688478
1000 genomesrs149688478
hgdprs149688478
ensemblrs149688478
gopubmedrs149688478
geneviewrs149688478
scholarrs149688478
googlers149688478
pharmgkbrs149688478
gwascentralrs149688478
openSNPrs149688478
23andMers149688478
23andMe allrs149688478
SNP Nexus

SNPshotrs149688478
SNPdbers149688478
MSV3drs149688478
GWAS Ctlgrs149688478
Max Magnitude0
ClinVar
Risk rs149688478(A;A)
Alt rs149688478(A;A)
Reference rs149688478(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SPATA5
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.123868644G>A
CLNSRC
CLNACC RCV000190099.1,