rs1057524877

Orientation

minus

Stabilized

minus

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

Make rs1057524877(A;G)

Make rs1057524877(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

21

Position

32657036

Gene

SYNJ1

is a	snp
is	mentioned by
dbSNP	rs1057524877
dbSNP (classic)	rs1057524877
ClinGen	rs1057524877
ebi	rs1057524877
HLI	rs1057524877
Exac	rs1057524877
Gnomad	rs1057524877
Varsome	rs1057524877
LitVar	rs1057524877
Map	rs1057524877
PheGenI	rs1057524877
Biobank	rs1057524877
1000 genomes	rs1057524877
hgdp	rs1057524877
ensembl	rs1057524877
geneview	rs1057524877
scholar	rs1057524877
google	rs1057524877
pharmgkb	rs1057524877
gwascentral	rs1057524877
openSNP	rs1057524877
23andMe	rs1057524877
SNPshot	rs1057524877
SNPdbe	rs1057524877
MSV3d	rs1057524877
GWAS Ctlg	rs1057524877

Max Magnitude

0

ClinVar
Risk	rs1057524877(G;G)
Alt	rs1057524877(G;G)
Reference	Rs1057524877(A;A)
Significance	Pathogenic
Disease	Epileptic encephalopathy
Variation	info
Gene	SYNJ1
CLNDBN	Epileptic encephalopathy, early infantile, 53
Reversed	1
HGVS	NC_000021.8:g.34029346T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000445434.1,