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rs796053338

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053338(C;C)
Make rs796053338(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position128632302
GeneSPTAN1
is asnp
is mentioned by
dbSNPrs796053338
ebirs796053338
HLIrs796053338
Exacrs796053338
Varsomers796053338
Maprs796053338
PheGenIrs796053338
hapmaprs796053338
1000 genomesrs796053338
hgdprs796053338
ensemblrs796053338
gopubmedrs796053338
geneviewrs796053338
scholarrs796053338
googlers796053338
pharmgkbrs796053338
gwascentralrs796053338
openSNPrs796053338
23andMers796053338
23andMe allrs796053338
SNP Nexus

SNPshotrs796053338
SNPdbers796053338
MSV3drs796053338
GWAS Ctlgrs796053338
Max Magnitude0
ClinVar
Risk rs796053338(C;C)
Alt rs796053338(C;C)
Reference rs796053338(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPTAN1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.131394581T>C
CLNSRC
CLNACC RCV000189553.1,