rs1057524761

Orientation

minus

Stabilized

minus

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

Make rs1057524761(A;A)

Make rs1057524761(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

66714359

Gene

SPTBN2

is a	snp
is	mentioned by
dbSNP	rs1057524761
dbSNP (classic)	rs1057524761
ClinGen	rs1057524761
ebi	rs1057524761
HLI	rs1057524761
Exac	rs1057524761
Gnomad	rs1057524761
Varsome	rs1057524761
LitVar	rs1057524761
Map	rs1057524761
PheGenI	rs1057524761
Biobank	rs1057524761
1000 genomes	rs1057524761
hgdp	rs1057524761
ensembl	rs1057524761
geneview	rs1057524761
scholar	rs1057524761
google	rs1057524761
pharmgkb	rs1057524761
gwascentral	rs1057524761
openSNP	rs1057524761
23andMe	rs1057524761
SNPshot	rs1057524761
SNPdbe	rs1057524761
MSV3d	rs1057524761
GWAS Ctlg	rs1057524761

Max Magnitude

0

ClinVar
Risk	rs1057524761(A;A)
Alt	rs1057524761(A;A)
Reference	Rs1057524761(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SPTBN2
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.66481830C>T
CLNSRC
CLNACC	RCV000423934.1,