rs797044892

Orientation

minus

Stabilized

minus

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

Make rs797044892(C;C)

Make rs797044892(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

21805938

Gene

MAPK1

is a	snp
is	mentioned by
dbSNP	rs797044892
dbSNP (classic)	rs797044892
ClinGen	rs797044892
ebi	rs797044892
HLI	rs797044892
Exac	rs797044892
Gnomad	rs797044892
Varsome	rs797044892
LitVar	rs797044892
Map	rs797044892
PheGenI	rs797044892
Biobank	rs797044892
1000 genomes	rs797044892
hgdp	rs797044892
ensembl	rs797044892
geneview	rs797044892
scholar	rs797044892
google	rs797044892
pharmgkb	rs797044892
gwascentral	rs797044892
openSNP	rs797044892
23andMe	rs797044892
SNPshot	rs797044892
SNPdbe	rs797044892
MSV3d	rs797044892
GWAS Ctlg	rs797044892

Max Magnitude

0

ClinVar
Risk	rs797044892(C;C)
Alt	rs797044892(C;C)
Reference	Rs797044892(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	MAPK1
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000022.10:g.22160227C>G
CLNSRC
CLNACC	RCV000190714.1,