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

rs796053327

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053327(A;T)
Make rs796053327(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position128632263
GeneSPTAN1
is asnp
is mentioned by
dbSNPrs796053327
ebirs796053327
HLIrs796053327
Exacrs796053327
Varsomers796053327
Maprs796053327
PheGenIrs796053327
hapmaprs796053327
1000 genomesrs796053327
hgdprs796053327
ensemblrs796053327
gopubmedrs796053327
geneviewrs796053327
scholarrs796053327
googlers796053327
pharmgkbrs796053327
gwascentralrs796053327
openSNPrs796053327
23andMers796053327
23andMe allrs796053327
SNP Nexus

SNPshotrs796053327
SNPdbers796053327
MSV3drs796053327
GWAS Ctlgrs796053327
Max Magnitude0
ClinVar
Risk rs796053327(T;T)
Alt rs796053327(T;T)
Reference rs796053327(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPTAN1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.131394542A>T
CLNSRC
CLNACC RCV000189533.2,