rs1057522832

Orientation

minus

Stabilized

minus

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

Make rs1057522832(C;C)

Make rs1057522832(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

55015586

Gene

ALAS2

is a	snp
is	mentioned by
dbSNP	rs1057522832
dbSNP (classic)	rs1057522832
ClinGen	rs1057522832
ebi	rs1057522832
HLI	rs1057522832
Exac	rs1057522832
Gnomad	rs1057522832
Varsome	rs1057522832
LitVar	rs1057522832
Map	rs1057522832
PheGenI	rs1057522832
Biobank	rs1057522832
1000 genomes	rs1057522832
hgdp	rs1057522832
ensembl	rs1057522832
geneview	rs1057522832
scholar	rs1057522832
google	rs1057522832
pharmgkb	rs1057522832
gwascentral	rs1057522832
openSNP	rs1057522832
23andMe	rs1057522832
SNPshot	rs1057522832
SNPdbe	rs1057522832
MSV3d	rs1057522832
GWAS Ctlg	rs1057522832

Max Magnitude

0

ClinVar
Risk	rs1057522832(C;C)
Alt	rs1057522832(C;C)
Reference	Rs1057522832(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ALAS2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.55042019C>G
CLNSRC
CLNACC	RCV000428069.1,