rs267607176

Orientation

plus

Stabilized

plus

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

Make rs267607176(C;C)

Make rs267607176(C;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

36067415

Gene

WDR62

is a	snp
is	mentioned by
dbSNP	rs267607176
dbSNP (classic)	rs267607176
ClinGen	rs267607176
ebi	rs267607176
HLI	rs267607176
Exac	rs267607176
Gnomad	rs267607176
Varsome	rs267607176
LitVar	rs267607176
Map	rs267607176
PheGenI	rs267607176
Biobank	rs267607176
1000 genomes	rs267607176
hgdp	rs267607176
ensembl	rs267607176
geneview	rs267607176
scholar	rs267607176
google	rs267607176
pharmgkb	rs267607176
gwascentral	rs267607176
openSNP	rs267607176
23andMe	rs267607176
SNPshot	rs267607176
SNPdbe	rs267607176
MSV3d	rs267607176
GWAS Ctlg	rs267607176

Max Magnitude

0

ClinVar
Risk	rs267607176(C;C)
Alt	rs267607176(C;C)
Reference	Rs267607176(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.36558317G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000000059.4,