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rs796052243

From SNPedia

Orientationplus
Geno Mag Summary
(CAA;CAA) 0 common in clinvar
Make rs796052243(-;-)
Make rs796052243(-;CAA)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position122934580
GeneSPATA5
is asnp
is mentioned by
dbSNPrs796052243
ebirs796052243
HLIrs796052243
Exacrs796052243
Varsomers796052243
Maprs796052243
PheGenIrs796052243
hapmaprs796052243
1000 genomesrs796052243
hgdprs796052243
ensemblrs796052243
gopubmedrs796052243
geneviewrs796052243
scholarrs796052243
googlers796052243
pharmgkbrs796052243
gwascentralrs796052243
openSNPrs796052243
23andMers796052243
23andMe allrs796052243
SNP Nexus

SNPshotrs796052243
SNPdbers796052243
MSV3drs796052243
GWAS Ctlgrs796052243
Max Magnitude0
ClinVar
Risk rs796052243(;)
Alt rs796052243(;)
Reference rs796052243(CAA;CAA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPATA5
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.123855735_123855737delCAA
CLNSRC
CLNACC RCV000190122.1,