rs387907084

Orientation

plus

Stabilized

plus

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

Make rs387907084(A;A)

Make rs387907084(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

36058795

Gene

WDR62

is a	snp
is	mentioned by
dbSNP	rs387907084
dbSNP (classic)	rs387907084
ClinGen	rs387907084
ebi	rs387907084
HLI	rs387907084
Exac	rs387907084
Gnomad	rs387907084
Varsome	rs387907084
LitVar	rs387907084
Map	rs387907084
PheGenI	rs387907084
Biobank	rs387907084
1000 genomes	rs387907084
hgdp	rs387907084
ensembl	rs387907084
geneview	rs387907084
scholar	rs387907084
google	rs387907084
pharmgkb	rs387907084
gwascentral	rs387907084
openSNP	rs387907084
23andMe	rs387907084
SNPshot	rs387907084
SNPdbe	rs387907084
MSV3d	rs387907084
GWAS Ctlg	rs387907084

Max Magnitude

0

ClinVar
Risk	rs387907084(A;A)
Alt	rs387907084(A;A)
Reference	Rs387907084(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.36549697G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000024034.4,