rs796053334

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(I;I)	0	common genotype

Make rs796053334(-;CAGCTGGGC)

Make rs796053334(CAGCTGGGC;CAGCTGGGC)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

128632282

Gene

SPTAN1

is a	snp
is	mentioned by
dbSNP	rs796053334
dbSNP (classic)	rs796053334
ClinGen	rs796053334
ebi	rs796053334
HLI	rs796053334
Exac	rs796053334
Gnomad	rs796053334
Varsome	rs796053334
LitVar	rs796053334
Map	rs796053334
PheGenI	rs796053334
Biobank	rs796053334
1000 genomes	rs796053334
hgdp	rs796053334
ensembl	rs796053334
geneview	rs796053334
scholar	rs796053334
google	rs796053334
pharmgkb	rs796053334
gwascentral	rs796053334
openSNP	rs796053334
23andMe	rs796053334
SNPshot	rs796053334
SNPdbe	rs796053334
MSV3d	rs796053334
GWAS Ctlg	rs796053334

Max Magnitude

0

ClinVar
Risk	rs796053334(CCAGCTGGG;CCAGCTGGG)
Alt	rs796053334(CCAGCTGGG;CCAGCTGGG)
Reference	Rs796053334(-;-)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SPTAN1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.131394553_131394561dupCAGCTGGGC
CLNSRC
CLNACC	RCV000189544.1,