rs1057518078

Orientation

plus

Stabilized

plus

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

Make rs1057518078(-;-)

Make rs1057518078(-;TGGGAGAACTGAAGG)

Make rs1057518078(TGGGAGAACTGAAGG;TGGGAGAACTGAAGG)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

66435125

Gene

MAP2K1

is a	snp
is	mentioned by
dbSNP	rs1057518078
dbSNP (classic)	rs1057518078
ClinGen	rs1057518078
ebi	rs1057518078
HLI	rs1057518078
Exac	rs1057518078
Gnomad	rs1057518078
Varsome	rs1057518078
LitVar	rs1057518078
Map	rs1057518078
PheGenI	rs1057518078
Biobank	rs1057518078
1000 genomes	rs1057518078
hgdp	rs1057518078
ensembl	rs1057518078
geneview	rs1057518078
scholar	rs1057518078
google	rs1057518078
pharmgkb	rs1057518078
gwascentral	rs1057518078
openSNP	rs1057518078
23andMe	rs1057518078
SNPshot	rs1057518078
SNPdbe	rs1057518078
MSV3d	rs1057518078
GWAS Ctlg	rs1057518078

Max Magnitude

0

ClinVar
Risk	rs1057518078(-;-)
Alt	rs1057518078(-;-)
Reference	Rs1057518078(GAAGGTGGGAGAACT;GAAGGTGGGAGAACT)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MAP2K1
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.66727463_66727477delTGGGAGAACTGAAGG
CLNSRC
CLNACC	RCV000413847.1,