rs863223905

Orientation

minus

Stabilized

minus

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

Make rs863223905(A;G)

Make rs863223905(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

55015667

Gene

ALAS2

is a	snp
is	mentioned by
dbSNP	rs863223905
dbSNP (classic)	rs863223905
ClinGen	rs863223905
ebi	rs863223905
HLI	rs863223905
Exac	rs863223905
Gnomad	rs863223905
Varsome	rs863223905
LitVar	rs863223905
Map	rs863223905
PheGenI	rs863223905
Biobank	rs863223905
1000 genomes	rs863223905
hgdp	rs863223905
ensembl	rs863223905
geneview	rs863223905
scholar	rs863223905
google	rs863223905
pharmgkb	rs863223905
gwascentral	rs863223905
openSNP	rs863223905
23andMe	rs863223905
SNPshot	rs863223905
SNPdbe	rs863223905
MSV3d	rs863223905
GWAS Ctlg	rs863223905

Max Magnitude

0

ClinVar
Risk	rs863223905(G;G)
Alt	rs863223905(G;G)
Reference	Rs863223905(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ALAS2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.55042100T>C
CLNSRC
CLNACC	RCV000198893.1,