rs796053338

Orientation

plus

Stabilized

plus

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

Make rs796053338(C;C)

Make rs796053338(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

128632302

Gene

SPTAN1

is a	snp
is	mentioned by
dbSNP	rs796053338
dbSNP (classic)	rs796053338
ClinGen	rs796053338
ebi	rs796053338
HLI	rs796053338
Exac	rs796053338
Gnomad	rs796053338
Varsome	rs796053338
LitVar	rs796053338
Map	rs796053338
PheGenI	rs796053338
Biobank	rs796053338
1000 genomes	rs796053338
hgdp	rs796053338
ensembl	rs796053338
geneview	rs796053338
scholar	rs796053338
google	rs796053338
pharmgkb	rs796053338
gwascentral	rs796053338
openSNP	rs796053338
23andMe	rs796053338
SNPshot	rs796053338
SNPdbe	rs796053338
MSV3d	rs796053338
GWAS Ctlg	rs796053338

Max Magnitude

0

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,