rs863223906

Orientation

minus

Stabilized

minus

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

Make rs863223906(A;G)

Make rs863223906(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

55009245

Gene

ALAS2

is a	snp
is	mentioned by
dbSNP	rs863223906
dbSNP (classic)	rs863223906
ClinGen	rs863223906
ebi	rs863223906
HLI	rs863223906
Exac	rs863223906
Gnomad	rs863223906
Varsome	rs863223906
LitVar	rs863223906
Map	rs863223906
PheGenI	rs863223906
Biobank	rs863223906
1000 genomes	rs863223906
hgdp	rs863223906
ensembl	rs863223906
geneview	rs863223906
scholar	rs863223906
google	rs863223906
pharmgkb	rs863223906
gwascentral	rs863223906
openSNP	rs863223906
23andMe	rs863223906
SNPshot	rs863223906
SNPdbe	rs863223906
MSV3d	rs863223906
GWAS Ctlg	rs863223906

Max Magnitude

0

ClinVar
Risk	rs863223906(G;G)
Alt	rs863223906(G;G)
Reference	Rs863223906(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ALAS2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.55035678T>C
CLNSRC
CLNACC	RCV000195971.1,