rs267607177

Orientation

plus

Stabilized

plus

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

Make rs267607177(C;T)

Make rs267607177(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

36083099

Gene

WDR62

is a	snp
is	mentioned by
dbSNP	rs267607177
dbSNP (classic)	rs267607177
ClinGen	rs267607177
ebi	rs267607177
HLI	rs267607177
Exac	rs267607177
Gnomad	rs267607177
Varsome	rs267607177
LitVar	rs267607177
Map	rs267607177
PheGenI	rs267607177
Biobank	rs267607177
1000 genomes	rs267607177
hgdp	rs267607177
ensembl	rs267607177
geneview	rs267607177
scholar	rs267607177
google	rs267607177
pharmgkb	rs267607177
gwascentral	rs267607177
openSNP	rs267607177
23andMe	rs267607177
SNPshot	rs267607177
SNPdbe	rs267607177
MSV3d	rs267607177
GWAS Ctlg	rs267607177

Max Magnitude

0

ClinVar
Risk	rs267607177(T;T)
Alt	rs267607177(T;T)
Reference	Rs267607177(C;C)
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.36574001C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000060.3,