Have questions? Visit https://www.reddit.com/r/SNPedia

rs796053321

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053321(A;C)
Make rs796053321(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position128618934
GeneSPTAN1
is asnp
is mentioned by
dbSNPrs796053321
ebirs796053321
HLIrs796053321
Exacrs796053321
Varsomers796053321
Maprs796053321
PheGenIrs796053321
hapmaprs796053321
1000 genomesrs796053321
hgdprs796053321
ensemblrs796053321
gopubmedrs796053321
geneviewrs796053321
scholarrs796053321
googlers796053321
pharmgkbrs796053321
gwascentralrs796053321
openSNPrs796053321
23andMers796053321
23andMe allrs796053321
SNP Nexus

SNPshotrs796053321
SNPdbers796053321
MSV3drs796053321
GWAS Ctlgrs796053321
Max Magnitude0
ClinVar
Risk rs796053321(C;C)
Alt rs796053321(C;C)
Reference rs796053321(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPTAN1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.131381213A>C
CLNSRC
CLNACC RCV000189519.1,