rs547204431

Orientation

plus

Stabilized

plus

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

Make rs547204431(G;T)

Make rs547204431(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

192810432

Gene

RGS2

is a	snp
is	mentioned by
dbSNP	rs547204431
dbSNP (classic)	rs547204431
ClinGen	rs547204431
ebi	rs547204431
HLI	rs547204431
Exac	rs547204431
Gnomad	rs547204431
Varsome	rs547204431
LitVar	rs547204431
Map	rs547204431
PheGenI	rs547204431
Biobank	rs547204431
1000 genomes	rs547204431
hgdp	rs547204431
ensembl	rs547204431
geneview	rs547204431
scholar	rs547204431
google	rs547204431
pharmgkb	rs547204431
gwascentral	rs547204431
openSNP	rs547204431
23andMe	rs547204431
SNPshot	rs547204431
SNPdbe	rs547204431
MSV3d	rs547204431
GWAS Ctlg	rs547204431

Max Magnitude

0

ClinVar
Risk	rs547204431(T;T)
Alt	rs547204431(T;T)
Reference	Rs547204431(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RGS2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.192779562G>T
CLNSRC
CLNACC	RCV000412916.1,