rs863223322

Orientation

plus

Stabilized

plus

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

Make rs863223322(-;-)

Make rs863223322(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

36091251

Gene

WDR62

is a	snp
is	mentioned by
dbSNP	rs863223322
dbSNP (classic)	rs863223322
ClinGen	rs863223322
ebi	rs863223322
HLI	rs863223322
Exac	rs863223322
Gnomad	rs863223322
Varsome	rs863223322
LitVar	rs863223322
Map	rs863223322
PheGenI	rs863223322
Biobank	rs863223322
1000 genomes	rs863223322
hgdp	rs863223322
ensembl	rs863223322
geneview	rs863223322
scholar	rs863223322
google	rs863223322
pharmgkb	rs863223322
gwascentral	rs863223322
openSNP	rs863223322
23andMe	rs863223322
SNPshot	rs863223322
SNPdbe	rs863223322
MSV3d	rs863223322
GWAS Ctlg	rs863223322

Max Magnitude

0

ClinVar
Risk	rs863223322(-;-)
Alt	rs863223322(-;-)
Reference	Rs863223322(A;A)
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.36582153delA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000024035.4,