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rs796051894

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051894(A;A)
Make rs796051894(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position123256026
GeneSPATA5
is asnp
is mentioned by
dbSNPrs796051894
ebirs796051894
HLIrs796051894
Exacrs796051894
Varsomers796051894
Maprs796051894
PheGenIrs796051894
hapmaprs796051894
1000 genomesrs796051894
hgdprs796051894
ensemblrs796051894
gopubmedrs796051894
geneviewrs796051894
scholarrs796051894
googlers796051894
pharmgkbrs796051894
gwascentralrs796051894
openSNPrs796051894
23andMers796051894
23andMe allrs796051894
SNP Nexus

SNPshotrs796051894
SNPdbers796051894
MSV3drs796051894
GWAS Ctlgrs796051894
Max Magnitude0
ClinVar
Risk rs796051894(A;A)
Alt rs796051894(A;A)
Reference rs796051894(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SPATA5
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.124177181G>A
CLNSRC
CLNACC RCV000185656.1,