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rs796051893

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051893(G;T)
Make rs796051893(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position122927739
GeneSPATA5
is asnp
is mentioned by
dbSNPrs796051893
ebirs796051893
HLIrs796051893
Exacrs796051893
Varsomers796051893
Maprs796051893
PheGenIrs796051893
hapmaprs796051893
1000 genomesrs796051893
hgdprs796051893
ensemblrs796051893
gopubmedrs796051893
geneviewrs796051893
scholarrs796051893
googlers796051893
pharmgkbrs796051893
gwascentralrs796051893
openSNPrs796051893
23andMers796051893
23andMe allrs796051893
SNP Nexus

SNPshotrs796051893
SNPdbers796051893
MSV3drs796051893
GWAS Ctlgrs796051893
Max Magnitude0
ClinVar
Risk rs796051893(T;T)
Alt rs796051893(T;T)
Reference rs796051893(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SPATA5
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.123848894G>T
CLNSRC
CLNACC RCV000185655.1,