rs587784553

Orientation

plus

Stabilized

plus

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

Make rs587784553(A;A)

Make rs587784553(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

36060031

Gene

WDR62

is a	snp
is	mentioned by
dbSNP	rs587784553
dbSNP (classic)	rs587784553
ClinGen	rs587784553
ebi	rs587784553
HLI	rs587784553
Exac	rs587784553
Gnomad	rs587784553
Varsome	rs587784553
LitVar	rs587784553
Map	rs587784553
PheGenI	rs587784553
Biobank	rs587784553
1000 genomes	rs587784553
hgdp	rs587784553
ensembl	rs587784553
geneview	rs587784553
scholar	rs587784553
google	rs587784553
pharmgkb	rs587784553
gwascentral	rs587784553
openSNP	rs587784553
23andMe	rs587784553
SNPshot	rs587784553
SNPdbe	rs587784553
MSV3d	rs587784553
GWAS Ctlg	rs587784553

Max Magnitude

0

ClinVar
Risk	rs587784553(A;A)
Alt	rs587784553(A;A)
Reference	Rs587784553(G;G)
Significance	Pathogenic
Disease	Primary autosomal recessive microcephaly 2
Variation	info
Gene	WDR62
CLNDBN	Primary autosomal recessive microcephaly 2
Reversed	0
HGVS	NC_000019.9:g.36550933G>A
CLNSRC
CLNACC	RCV000147952.1,