rs376633424

Orientation

plus

Stabilized

plus

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

Make rs376633424(C;T)

Make rs376633424(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

36102820

Gene

WDR62

is a	snp
is	mentioned by
dbSNP	rs376633424
dbSNP (classic)	rs376633424
ClinGen	rs376633424
ebi	rs376633424
HLI	rs376633424
Exac	rs376633424
Gnomad	rs376633424
Varsome	rs376633424
LitVar	rs376633424
Map	rs376633424
PheGenI	rs376633424
Biobank	rs376633424
1000 genomes	rs376633424
hgdp	rs376633424
ensembl	rs376633424
geneview	rs376633424
scholar	rs376633424
google	rs376633424
pharmgkb	rs376633424
gwascentral	rs376633424
openSNP	rs376633424
23andMe	rs376633424
SNPshot	rs376633424
SNPdbe	rs376633424
MSV3d	rs376633424
GWAS Ctlg	rs376633424

Max Magnitude

0

ClinVar
Risk	rs376633424(T;T)
Alt	rs376633424(T;T)
Reference	Rs376633424(C;C)
Significance	Pathogenic
Disease	Abnormality of neuronal migration
Variation	info
Gene	WDR62
CLNDBN	Abnormality of neuronal migration
Reversed	0
HGVS	NC_000019.9:g.36593722C>T
CLNSRC
CLNACC	RCV000201333.1,