rs28940281

Orientation

plus

Stabilized

plus

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

Make rs28940281(C;T)

Make rs28940281(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

1882669

Gene

ARHGEF10

is a	snp
is	mentioned by
dbSNP	rs28940281
dbSNP (classic)	rs28940281
ClinGen	rs28940281
ebi	rs28940281
HLI	rs28940281
Exac	rs28940281
Gnomad	rs28940281
Varsome	rs28940281
LitVar	rs28940281
Map	rs28940281
PheGenI	rs28940281
Biobank	rs28940281
1000 genomes	rs28940281
hgdp	rs28940281
ensembl	rs28940281
geneview	rs28940281
scholar	rs28940281
google	rs28940281
pharmgkb	rs28940281
gwascentral	rs28940281
openSNP	rs28940281
23andMe	rs28940281
SNPshot	rs28940281
SNPdbe	rs28940281
MSV3d	rs28940281
GWAS Ctlg	rs28940281

Max Magnitude

0

OMIM	608136
Desc	SLOWED NERVE CONDUCTION VELOCITY, AUTOSOMAL DOMINANT
Variant	0001
Related	also

ClinVar
Risk	rs28940281(T;T)
Alt	rs28940281(T;T)
Reference	Rs28940281(C;C)
Significance	Pathogenic
Disease	Slowed nerve conduction velocity
Variation	info
Gene	ARHGEF10
CLNDBN	Slowed nerve conduction velocity, autosomal dominant
Reversed	0
HGVS	NC_000008.10:g.1830835C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002634.4,