rs730880518

Orientation

minus

Stabilized

minus

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

Make rs730880518(G;T)

Make rs730880518(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

4117532

Gene

MAP2K2

is a	snp
is	mentioned by
dbSNP	rs730880518
dbSNP (classic)	rs730880518
ClinGen	rs730880518
ebi	rs730880518
HLI	rs730880518
Exac	rs730880518
Gnomad	rs730880518
Varsome	rs730880518
LitVar	rs730880518
Map	rs730880518
PheGenI	rs730880518
Biobank	rs730880518
1000 genomes	rs730880518
hgdp	rs730880518
ensembl	rs730880518
geneview	rs730880518
scholar	rs730880518
google	rs730880518
pharmgkb	rs730880518
gwascentral	rs730880518
openSNP	rs730880518
23andMe	rs730880518
SNPshot	rs730880518
SNPdbe	rs730880518
MSV3d	rs730880518
GWAS Ctlg	rs730880518

Max Magnitude

0

ClinVar
Risk	rs730880518(T;T)
Alt	rs730880518(T;T)
Reference	Rs730880518(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MAP2K2
CLNDBN	not provided
Reversed	1
HGVS	NC_000019.9:g.4117530C>A
CLNSRC
CLNACC	RCV000158040.1,