rs774923951

Orientation

plus

Stabilized

plus

Make rs774923951(C;C)

Make rs774923951(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

6

Position

87589957

Gene	ORC3, RARS2

is a	snp
is	mentioned by
dbSNP	rs774923951
dbSNP (classic)	rs774923951
ClinGen	rs774923951
ebi	rs774923951
HLI	rs774923951
Exac	rs774923951
Gnomad	rs774923951
Varsome	rs774923951
LitVar	rs774923951
Map	rs774923951
PheGenI	rs774923951
Biobank	rs774923951
1000 genomes	rs774923951
hgdp	rs774923951
ensembl	rs774923951
geneview	rs774923951
scholar	rs774923951
google	rs774923951
pharmgkb	rs774923951
gwascentral	rs774923951
openSNP	rs774923951
23andMe	rs774923951
SNPshot	rs774923951
SNPdbe	rs774923951
MSV3d	rs774923951
GWAS Ctlg	rs774923951

Max Magnitude

0

ClinVar
Risk	rs774923951(A;A) rs774923951(C;C) rs774923951(G;G)
Alt	rs774923951(A;A) rs774923951(C;C) rs774923951(G;G)
Reference	Rs774923951(T;T)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	RARS2 ORC3
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000006.11:g.88299675T>C
CLNSRC
CLNACC	RCV000210553.1,