rs539555837

Orientation

plus

Stabilized

plus

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

Make rs539555837(C;C)

Make rs539555837(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

4099302

Gene

MAP2K2

is a	snp
is	mentioned by
dbSNP	rs539555837
dbSNP (classic)	rs539555837
ClinGen	rs539555837
ebi	rs539555837
HLI	rs539555837
Exac	rs539555837
Gnomad	rs539555837
Varsome	rs539555837
LitVar	rs539555837
Map	rs539555837
PheGenI	rs539555837
Biobank	rs539555837
1000 genomes	rs539555837
hgdp	rs539555837
ensembl	rs539555837
geneview	rs539555837
scholar	rs539555837
google	rs539555837
pharmgkb	rs539555837
gwascentral	rs539555837
openSNP	rs539555837
23andMe	rs539555837
SNPshot	rs539555837
SNPdbe	rs539555837
MSV3d	rs539555837
GWAS Ctlg	rs539555837

Max Magnitude

0

ClinVar
Risk	rs539555837(C;C)
Alt	rs539555837(C;C)
Reference	Rs539555837(T;T)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	MAP2K2
CLNDBN	not specified
Reversed	0
HGVS	NC_000019.9:g.4099300T>C
CLNSRC
CLNACC	RCV000158027.2,