rs797044873

Orientation

plus

Stabilized

plus

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

Make rs797044873(G;T)

Make rs797044873(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

10284751

Gene

SNAP25

is a	snp
is	mentioned by
dbSNP	rs797044873
dbSNP (classic)	rs797044873
ClinGen	rs797044873
ebi	rs797044873
HLI	rs797044873
Exac	rs797044873
Gnomad	rs797044873
Varsome	rs797044873
LitVar	rs797044873
Map	rs797044873
PheGenI	rs797044873
Biobank	rs797044873
1000 genomes	rs797044873
hgdp	rs797044873
ensembl	rs797044873
geneview	rs797044873
scholar	rs797044873
google	rs797044873
pharmgkb	rs797044873
gwascentral	rs797044873
openSNP	rs797044873
23andMe	rs797044873
SNPshot	rs797044873
SNPdbe	rs797044873
MSV3d	rs797044873
GWAS Ctlg	rs797044873

Max Magnitude

0

ClinVar
Risk	rs797044873(T;T)
Alt	rs797044873(T;T)
Reference	Rs797044873(G;G)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	SNAP25
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000020.10:g.10265399G>T
CLNSRC
CLNACC	RCV000190683.1,