rs145129059

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs145129059(C;G)

Make rs145129059(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

128625802

Gene

SPTAN1

is a	snp
is	mentioned by
dbSNP	rs145129059
dbSNP (classic)	rs145129059
ClinGen	rs145129059
ebi	rs145129059
HLI	rs145129059
Exac	rs145129059
Gnomad	rs145129059
Varsome	rs145129059
LitVar	rs145129059
Map	rs145129059
PheGenI	rs145129059
Biobank	rs145129059
1000 genomes	rs145129059
hgdp	rs145129059
ensembl	rs145129059
geneview	rs145129059
scholar	rs145129059
google	rs145129059
pharmgkb	rs145129059
gwascentral	rs145129059
openSNP	rs145129059
23andMe	rs145129059
SNPshot	rs145129059
SNPdbe	rs145129059
MSV3d	rs145129059
GWAS Ctlg	rs145129059

Max Magnitude

0

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,