rs786204766

Orientation

minus

Stabilized

minus

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

Make rs786204766(A;A)

Make rs786204766(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

64794466

Gene

SPTB

is a	snp
is	mentioned by
dbSNP	rs786204766
dbSNP (classic)	rs786204766
ClinGen	rs786204766
ebi	rs786204766
HLI	rs786204766
Exac	rs786204766
Gnomad	rs786204766
Varsome	rs786204766
LitVar	rs786204766
Map	rs786204766
PheGenI	rs786204766
Biobank	rs786204766
1000 genomes	rs786204766
hgdp	rs786204766
ensembl	rs786204766
geneview	rs786204766
scholar	rs786204766
google	rs786204766
pharmgkb	rs786204766
gwascentral	rs786204766
openSNP	rs786204766
23andMe	rs786204766
SNPshot	rs786204766
SNPdbe	rs786204766
MSV3d	rs786204766
GWAS Ctlg	rs786204766

Max Magnitude

0

ClinVar
Risk	rs786204766(A;A)
Alt	rs786204766(A;A)
Reference	Rs786204766(G;G)
Significance	Probable-Pathogenic
Disease	Spherocytosis type 2
Variation	info
Gene	SPTB
CLNDBN	Spherocytosis type 2
Reversed	1
HGVS	NC_000014.8:g.65261184C>T
CLNSRC
CLNACC	RCV000169630.1,