rs147875659

Orientation

plus

Stabilized

plus

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

Make rs147875659(A;A)

Make rs147875659(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

36084678

Gene

WDR62

is a	snp
is	mentioned by
dbSNP	rs147875659
dbSNP (classic)	rs147875659
ClinGen	rs147875659
ebi	rs147875659
HLI	rs147875659
Exac	rs147875659
Gnomad	rs147875659
Varsome	rs147875659
LitVar	rs147875659
Map	rs147875659
PheGenI	rs147875659
Biobank	rs147875659
1000 genomes	rs147875659
hgdp	rs147875659
ensembl	rs147875659
geneview	rs147875659
scholar	rs147875659
google	rs147875659
pharmgkb	rs147875659
gwascentral	rs147875659
openSNP	rs147875659
23andMe	rs147875659
SNPshot	rs147875659
SNPdbe	rs147875659
MSV3d	rs147875659
GWAS Ctlg	rs147875659

Max Magnitude

0

ClinVar
Risk	rs147875659(A;A)
Alt	rs147875659(A;A)
Reference	Rs147875659(G;G)
Significance	Other
Disease	Primary autosomal recessive microcephaly 2 not specified not provided
Variation	info
Gene	WDR62
CLNDBN	Primary autosomal recessive microcephaly 2 not specified not provided
Reversed	0
HGVS	NC_000019.9:g.36575580G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000000058.5, RCV000174280.1, RCV000489330.1,