rs587776899

Orientation

plus

Stabilized

plus

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

Make rs587776899(-;T)

Make rs587776899(T;T)

Reference

GRCh38 38.1/142

Chromosome

19

Position

36104605

Gene

WDR62

is a	snp
is	mentioned by
dbSNP	rs587776899
dbSNP (classic)	rs587776899
ClinGen	rs587776899
ebi	rs587776899
HLI	rs587776899
Exac	rs587776899
Gnomad	rs587776899
Varsome	rs587776899
LitVar	rs587776899
Map	rs587776899
PheGenI	rs587776899
Biobank	rs587776899
1000 genomes	rs587776899
hgdp	rs587776899
ensembl	rs587776899
geneview	rs587776899
scholar	rs587776899
google	rs587776899
pharmgkb	rs587776899
gwascentral	rs587776899
openSNP	rs587776899
23andMe	rs587776899
SNPshot	rs587776899
SNPdbe	rs587776899
MSV3d	rs587776899
GWAS Ctlg	rs587776899

Max Magnitude

0

ClinVar
Risk	rs587776899(T;T)
Alt	rs587776899(T;T)
Reference	Rs587776899(-;-)
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.36595507dupT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000024030.4,