rs876657651

Orientation

plus

Stabilized

plus

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

Make rs876657651(A;G)

Make rs876657651(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

15

Position

66436818

Gene

MAP2K1

is a	snp
is	mentioned by
dbSNP	rs876657651
dbSNP (classic)	rs876657651
ClinGen	rs876657651
ebi	rs876657651
HLI	rs876657651
Exac	rs876657651
Gnomad	rs876657651
Varsome	rs876657651
LitVar	rs876657651
Map	rs876657651
PheGenI	rs876657651
Biobank	rs876657651
1000 genomes	rs876657651
hgdp	rs876657651
ensembl	rs876657651
geneview	rs876657651
scholar	rs876657651
google	rs876657651
pharmgkb	rs876657651
gwascentral	rs876657651
openSNP	rs876657651
23andMe	rs876657651
SNPshot	rs876657651
SNPdbe	rs876657651
MSV3d	rs876657651
GWAS Ctlg	rs876657651

Max Magnitude

0

ClinVar
Risk	rs876657651(G;G)
Alt	rs876657651(G;G)
Reference	Rs876657651(A;A)
Significance	Probable-Pathogenic
Disease	Rasopathy
Variation	info
Gene	MAP2K1
CLNDBN	Rasopathy
Reversed	0
HGVS	NC_000015.9:g.66729156A>G
CLNSRC
CLNACC	RCV000220187.1,