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rs796052222

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052222(C;C)
Make rs796052222(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position123028194
GeneSPATA5
is asnp
is mentioned by
dbSNPrs796052222
ebirs796052222
HLIrs796052222
Exacrs796052222
Varsomers796052222
Maprs796052222
PheGenIrs796052222
hapmaprs796052222
1000 genomesrs796052222
hgdprs796052222
ensemblrs796052222
gopubmedrs796052222
geneviewrs796052222
scholarrs796052222
googlers796052222
pharmgkbrs796052222
gwascentralrs796052222
openSNPrs796052222
23andMers796052222
23andMe allrs796052222
SNP Nexus

SNPshotrs796052222
SNPdbers796052222
MSV3drs796052222
GWAS Ctlgrs796052222
Max Magnitude0
ClinVar
Risk rs796052222(C;C)
Alt rs796052222(C;C)
Reference rs796052222(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SPATA5
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.123949349G>C
CLNSRC
CLNACC RCV000190098.1,