rs869025339

Orientation

plus

Stabilized

plus

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

Make rs869025339(-;-)

Make rs869025339(-;AAG)

Make rs869025339(AAG;AAG)

Reference

GRCh38.p2 38.2/147

Chromosome

15

Position

66435121

Gene

MAP2K1

is a	snp
is	mentioned by
dbSNP	rs869025339
dbSNP (classic)	rs869025339
ClinGen	rs869025339
ebi	rs869025339
HLI	rs869025339
Exac	rs869025339
Gnomad	rs869025339
Varsome	rs869025339
LitVar	rs869025339
Map	rs869025339
PheGenI	rs869025339
Biobank	rs869025339
1000 genomes	rs869025339
hgdp	rs869025339
ensembl	rs869025339
geneview	rs869025339
scholar	rs869025339
google	rs869025339
pharmgkb	rs869025339
gwascentral	rs869025339
openSNP	rs869025339
23andMe	rs869025339
SNPshot	rs869025339
SNPdbe	rs869025339
MSV3d	rs869025339
GWAS Ctlg	rs869025339

Max Magnitude

0

ClinVar
Risk	rs869025339(-;-)
Alt	rs869025339(-;-)
Reference	Rs869025339(AGA;AGA)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MAP2K1
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.66727459_66727461delAAG
CLNSRC
CLNACC	RCV000207500.1,