rs587777420

Orientation

plus

Stabilized

plus

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

Make rs587777420(C;T)

Make rs587777420(T;T)

Reference

GRCh38 38.1/142

Chromosome

12

Position

8089982

Gene

NECAP1

is a	snp
is	mentioned by
dbSNP	rs587777420
dbSNP (classic)	rs587777420
ClinGen	rs587777420
ebi	rs587777420
HLI	rs587777420
Exac	rs587777420
Gnomad	rs587777420
Varsome	rs587777420
LitVar	rs587777420
Map	rs587777420
PheGenI	rs587777420
Biobank	rs587777420
1000 genomes	rs587777420
hgdp	rs587777420
ensembl	rs587777420
geneview	rs587777420
scholar	rs587777420
google	rs587777420
pharmgkb	rs587777420
gwascentral	rs587777420
openSNP	rs587777420
23andMe	rs587777420
SNPshot	rs587777420
SNPdbe	rs587777420
MSV3d	rs587777420
GWAS Ctlg	rs587777420

Max Magnitude

0

ClinVar
Risk	rs587777420(T;T)
Alt	rs587777420(T;T)
Reference	Rs587777420(C;C)
Significance	Other
Disease	Early infantile epileptic encephalopathy 21
Variation	info
Gene	NECAP1
CLNDBN	Early infantile epileptic encephalopathy 21
Reversed	0
HGVS	NC_000012.11:g.8242578C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000119841.3,