rs730880522

Orientation

minus

Stabilized

minus

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

Make rs730880522(A;A)

Make rs730880522(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

4099333

Gene

MAP2K2

is a	snp
is	mentioned by
dbSNP	rs730880522
dbSNP (classic)	rs730880522
ClinGen	rs730880522
ebi	rs730880522
HLI	rs730880522
Exac	rs730880522
Gnomad	rs730880522
Varsome	rs730880522
LitVar	rs730880522
Map	rs730880522
PheGenI	rs730880522
Biobank	rs730880522
1000 genomes	rs730880522
hgdp	rs730880522
ensembl	rs730880522
geneview	rs730880522
scholar	rs730880522
google	rs730880522
pharmgkb	rs730880522
gwascentral	rs730880522
openSNP	rs730880522
23andMe	rs730880522
SNPshot	rs730880522
SNPdbe	rs730880522
MSV3d	rs730880522
GWAS Ctlg	rs730880522

Max Magnitude

0

ClinVar
Risk	rs730880522(A;A)
Alt	rs730880522(A;A)
Reference	Rs730880522(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MAP2K2
CLNDBN	not provided
Reversed	1
HGVS	NC_000019.9:g.4099331C>T
CLNSRC
CLNACC	RCV000158047.2,