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rs145129059

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs145129059(C;G)
Make rs145129059(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position128625802
GeneSPTAN1
is asnp
is mentioned by
dbSNPrs145129059
ebirs145129059
HLIrs145129059
Exacrs145129059
Varsomers145129059
Maprs145129059
PheGenIrs145129059
hapmaprs145129059
1000 genomesrs145129059
hgdprs145129059
ensemblrs145129059
gopubmedrs145129059
geneviewrs145129059
scholarrs145129059
googlers145129059
pharmgkbrs145129059
gwascentralrs145129059
openSNPrs145129059
23andMers145129059
23andMe allrs145129059
SNP Nexus

SNPshotrs145129059
SNPdbers145129059
MSV3drs145129059
GWAS Ctlgrs145129059
Max Magnitude0
ClinVar
Risk rs145129059(G;G)
Alt rs145129059(G;G)
Reference rs145129059(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPTAN1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.131388081C>T
CLNSRC
CLNACC RCV000189521.1,