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rs796053332

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTC;CTC) 0 common in clinvar
Make rs796053332(-;-)
Make rs796053332(-;CTC)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position128585853
GeneSPTAN1
is asnp
is mentioned by
dbSNPrs796053332
ClinGenrs796053332
ebirs796053332
HLIrs796053332
Exacrs796053332
Varsomers796053332
Maprs796053332
PheGenIrs796053332
hapmaprs796053332
1000 genomesrs796053332
hgdprs796053332
ensemblrs796053332
gopubmedrs796053332
geneviewrs796053332
scholarrs796053332
googlers796053332
pharmgkbrs796053332
gwascentralrs796053332
openSNPrs796053332
23andMers796053332
23andMe allrs796053332
SNP Nexus

SNPshotrs796053332
SNPdbers796053332
MSV3drs796053332
GWAS Ctlgrs796053332
Max Magnitude0
ClinVar
Risk rs796053332(-;-)
Alt rs796053332(-;-)
Reference Rs796053332(CTC;CTC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPTAN1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.131348132_131348134delCTC
CLNSRC
CLNACC RCV000189541.1,