rs748232676

Orientation

plus

Stabilized

plus

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

Make rs748232676(A;A)

Make rs748232676(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

128566795

Gene

SPTAN1

is a	snp
is	mentioned by
dbSNP	rs748232676
dbSNP (classic)	rs748232676
ClinGen	rs748232676
ebi	rs748232676
HLI	rs748232676
Exac	rs748232676
Gnomad	rs748232676
Varsome	rs748232676
LitVar	rs748232676
Map	rs748232676
PheGenI	rs748232676
Biobank	rs748232676
1000 genomes	rs748232676
hgdp	rs748232676
ensembl	rs748232676
geneview	rs748232676
scholar	rs748232676
google	rs748232676
pharmgkb	rs748232676
gwascentral	rs748232676
openSNP	rs748232676
23andMe	rs748232676
SNPshot	rs748232676
SNPdbe	rs748232676
MSV3d	rs748232676
GWAS Ctlg	rs748232676

Max Magnitude

0

ClinVar
Risk	rs748232676(A;A) rs748232676(T;T)
Alt	rs748232676(A;A) rs748232676(T;T)
Reference	Rs748232676(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SPTAN1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.131329074C>T
CLNSRC
CLNACC	RCV000489427.1,