rs587776900

Orientation

plus

Stabilized

plus

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

Make rs587776900(-;C)

Make rs587776900(C;C)

Reference

GRCh38 38.1/142

Chromosome

19

Position

36103764

Gene

WDR62

is a	snp
is	mentioned by
dbSNP	rs587776900
dbSNP (classic)	rs587776900
ClinGen	rs587776900
ebi	rs587776900
HLI	rs587776900
Exac	rs587776900
Gnomad	rs587776900
Varsome	rs587776900
LitVar	rs587776900
Map	rs587776900
PheGenI	rs587776900
Biobank	rs587776900
1000 genomes	rs587776900
hgdp	rs587776900
ensembl	rs587776900
geneview	rs587776900
scholar	rs587776900
google	rs587776900
pharmgkb	rs587776900
gwascentral	rs587776900
openSNP	rs587776900
23andMe	rs587776900
SNPshot	rs587776900
SNPdbe	rs587776900
MSV3d	rs587776900
GWAS Ctlg	rs587776900

Max Magnitude

0

ClinVar
Risk	rs587776900(C;C)
Alt	rs587776900(C;C)
Reference	Rs587776900(-;-)
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.36594666dupC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000024032.5,