rs587776901

Orientation

plus

Stabilized

plus

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

Make rs587776901(-;-)

Make rs587776901(-;T)

Reference

GRCh38 38.1/142

Chromosome

19

Position

36065988

Gene

WDR62

is a	snp
is	mentioned by
dbSNP	rs587776901
dbSNP (classic)	rs587776901
ClinGen	rs587776901
ebi	rs587776901
HLI	rs587776901
Exac	rs587776901
Gnomad	rs587776901
Varsome	rs587776901
LitVar	rs587776901
Map	rs587776901
PheGenI	rs587776901
Biobank	rs587776901
1000 genomes	rs587776901
hgdp	rs587776901
ensembl	rs587776901
geneview	rs587776901
scholar	rs587776901
google	rs587776901
pharmgkb	rs587776901
gwascentral	rs587776901
openSNP	rs587776901
23andMe	rs587776901
SNPshot	rs587776901
SNPdbe	rs587776901
MSV3d	rs587776901
GWAS Ctlg	rs587776901

Max Magnitude

0

ClinVar
Risk	rs587776901(-;-)
Alt	rs587776901(-;-)
Reference	Rs587776901(T;T)
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.36556890delT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000024033.4,