rs863223901

Orientation

minus

Stabilized

minus

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

Make rs863223901(A;A)

Make rs863223901(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

55021084

Gene

ALAS2

is a	snp
is	mentioned by
dbSNP	rs863223901
dbSNP (classic)	rs863223901
ClinGen	rs863223901
ebi	rs863223901
HLI	rs863223901
Exac	rs863223901
Gnomad	rs863223901
Varsome	rs863223901
LitVar	rs863223901
Map	rs863223901
PheGenI	rs863223901
Biobank	rs863223901
1000 genomes	rs863223901
hgdp	rs863223901
ensembl	rs863223901
geneview	rs863223901
scholar	rs863223901
google	rs863223901
pharmgkb	rs863223901
gwascentral	rs863223901
openSNP	rs863223901
23andMe	rs863223901
SNPshot	rs863223901
SNPdbe	rs863223901
MSV3d	rs863223901
GWAS Ctlg	rs863223901

Max Magnitude

0

ClinVar
Risk	rs863223901(A;A)
Alt	rs863223901(A;A)
Reference	Rs863223901(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ALAS2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.55047517C>T
CLNSRC
CLNACC	RCV000198449.1,