rs587784558

Orientation

plus

Stabilized

plus

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

Make rs587784558(A;A)

Make rs587784558(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

36065984

Gene

WDR62

is a	snp
is	mentioned by
dbSNP	rs587784558
dbSNP (classic)	rs587784558
ClinGen	rs587784558
ebi	rs587784558
HLI	rs587784558
Exac	rs587784558
Gnomad	rs587784558
Varsome	rs587784558
LitVar	rs587784558
Map	rs587784558
PheGenI	rs587784558
Biobank	rs587784558
1000 genomes	rs587784558
hgdp	rs587784558
ensembl	rs587784558
geneview	rs587784558
scholar	rs587784558
google	rs587784558
pharmgkb	rs587784558
gwascentral	rs587784558
openSNP	rs587784558
23andMe	rs587784558
SNPshot	rs587784558
SNPdbe	rs587784558
MSV3d	rs587784558
GWAS Ctlg	rs587784558

Max Magnitude

0

ClinVar
Risk	rs587784558(A;A)
Alt	rs587784558(A;A)
Reference	Rs587784558(C;C)
Significance	Probable-Pathogenic
Disease	Primary autosomal recessive microcephaly 2
Variation	info
Gene	WDR62
CLNDBN	Primary autosomal recessive microcephaly 2
Reversed	0
HGVS	NC_000019.9:g.36556886C>A
CLNSRC
CLNACC	RCV000147962.1,