rs387906847

Orientation

minus

Stabilized

minus

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

Make rs387906847(A;G)

Make rs387906847(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

147952440

Gene

ORC4

is a	snp
is	mentioned by
dbSNP	rs387906847
dbSNP (classic)	rs387906847
ClinGen	rs387906847
ebi	rs387906847
HLI	rs387906847
Exac	rs387906847
Gnomad	rs387906847
Varsome	rs387906847
LitVar	rs387906847
Map	rs387906847
PheGenI	rs387906847
Biobank	rs387906847
1000 genomes	rs387906847
hgdp	rs387906847
ensembl	rs387906847
geneview	rs387906847
scholar	rs387906847
google	rs387906847
pharmgkb	rs387906847
gwascentral	rs387906847
openSNP	rs387906847
23andMe	rs387906847
SNPshot	rs387906847
SNPdbe	rs387906847
MSV3d	rs387906847
GWAS Ctlg	rs387906847

Max Magnitude

0

ClinVar
Risk	rs387906847(G;G)
Alt	rs387906847(G;G)
Reference	Rs387906847(A;A)
Significance	Other
Disease	Meier-Gorlin syndrome 2 not provided
Variation	info
Gene	ORC4
CLNDBN	Meier-Gorlin syndrome 2 not provided
Reversed	1
HGVS	NC_000002.11:g.148710009T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000023230.5, RCV000334756.1,