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rs796053328

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053328(C;T)
Make rs796053328(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position128632286
GeneSPTAN1
is asnp
is mentioned by
dbSNPrs796053328
ebirs796053328
HLIrs796053328
Exacrs796053328
Varsomers796053328
Maprs796053328
PheGenIrs796053328
hapmaprs796053328
1000 genomesrs796053328
hgdprs796053328
ensemblrs796053328
gopubmedrs796053328
geneviewrs796053328
scholarrs796053328
googlers796053328
pharmgkbrs796053328
gwascentralrs796053328
openSNPrs796053328
23andMers796053328
23andMe allrs796053328
SNP Nexus

SNPshotrs796053328
SNPdbers796053328
MSV3drs796053328
GWAS Ctlgrs796053328
Max Magnitude0
ClinVar
Risk rs796053328(T;T)
Alt rs796053328(T;T)
Reference rs796053328(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPTAN1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.131394565C>T
CLNSRC
CLNACC RCV000189534.1,