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rs567175477

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs567175477(A;A)
Make rs567175477(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position122947360
GeneSPATA5
is asnp
is mentioned by
dbSNPrs567175477
ebirs567175477
HLIrs567175477
Exacrs567175477
Varsomers567175477
Maprs567175477
PheGenIrs567175477
hapmaprs567175477
1000 genomesrs567175477
hgdprs567175477
ensemblrs567175477
gopubmedrs567175477
geneviewrs567175477
scholarrs567175477
googlers567175477
pharmgkbrs567175477
gwascentralrs567175477
openSNPrs567175477
23andMers567175477
23andMe allrs567175477
SNP Nexus

SNPshotrs567175477
SNPdbers567175477
MSV3drs567175477
GWAS Ctlgrs567175477
Max Magnitude0
ClinVar
Risk rs567175477(A;A)
Alt rs567175477(A;A)
Reference rs567175477(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SPATA5
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.123868515G>A
CLNSRC
CLNACC RCV000185647.1,