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

rs796053334

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796053334(-;CAGCTGGGC)
Make rs796053334(CAGCTGGGC;CAGCTGGGC)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position128632282
GeneSPTAN1
is asnp
is mentioned by
dbSNPrs796053334
ClinGenrs796053334
ebirs796053334
HLIrs796053334
Exacrs796053334
Varsomers796053334
Maprs796053334
PheGenIrs796053334
hapmaprs796053334
1000 genomesrs796053334
hgdprs796053334
ensemblrs796053334
gopubmedrs796053334
geneviewrs796053334
scholarrs796053334
googlers796053334
pharmgkbrs796053334
gwascentralrs796053334
openSNPrs796053334
23andMers796053334
23andMe allrs796053334
SNP Nexus

SNPshotrs796053334
SNPdbers796053334
MSV3drs796053334
GWAS Ctlgrs796053334
Max Magnitude0
ClinVar
Risk rs796053334(CCAGCTGGG;CCAGCTGGG)
Alt rs796053334(CCAGCTGGG;CCAGCTGGG)
Reference Rs796053334(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPTAN1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.131394553_131394561dupCAGCTGGGC
CLNSRC
CLNACC RCV000189544.1,