rs863223377

Orientation

plus

Stabilized

plus

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

Make rs863223377(C;C)

Make rs863223377(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

36090516

Gene

WDR62

is a	snp
is	mentioned by
dbSNP	rs863223377
dbSNP (classic)	rs863223377
ClinGen	rs863223377
ebi	rs863223377
HLI	rs863223377
Exac	rs863223377
Gnomad	rs863223377
Varsome	rs863223377
LitVar	rs863223377
Map	rs863223377
PheGenI	rs863223377
Biobank	rs863223377
1000 genomes	rs863223377
hgdp	rs863223377
ensembl	rs863223377
geneview	rs863223377
scholar	rs863223377
google	rs863223377
pharmgkb	rs863223377
gwascentral	rs863223377
openSNP	rs863223377
23andMe	rs863223377
SNPshot	rs863223377
SNPdbe	rs863223377
MSV3d	rs863223377
GWAS Ctlg	rs863223377

Max Magnitude

0

ClinVar
Risk	rs863223377(C;C)
Alt	rs863223377(C;C)
Reference	Rs863223377(T;T)
Significance	Pathogenic
Disease	Abnormality of neuronal migration
Variation	info
Gene	WDR62
CLNDBN	Abnormality of neuronal migration
Reversed	0
HGVS	NC_000019.9:g.36581418T>C
CLNSRC
CLNACC	RCV000201429.1,