rs863223902

Orientation

minus

Stabilized

minus

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

Make rs863223902(C;C)

Make rs863223902(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

55015653

Gene

ALAS2

is a	snp
is	mentioned by
dbSNP	rs863223902
dbSNP (classic)	rs863223902
ClinGen	rs863223902
ebi	rs863223902
HLI	rs863223902
Exac	rs863223902
Gnomad	rs863223902
Varsome	rs863223902
LitVar	rs863223902
Map	rs863223902
PheGenI	rs863223902
Biobank	rs863223902
1000 genomes	rs863223902
hgdp	rs863223902
ensembl	rs863223902
geneview	rs863223902
scholar	rs863223902
google	rs863223902
pharmgkb	rs863223902
gwascentral	rs863223902
openSNP	rs863223902
23andMe	rs863223902
SNPshot	rs863223902
SNPdbe	rs863223902
MSV3d	rs863223902
GWAS Ctlg	rs863223902

Max Magnitude

0

ClinVar
Risk	rs863223902(C;C)
Alt	rs863223902(C;C)
Reference	Rs863223902(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ALAS2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.55042086A>G
CLNSRC
CLNACC	RCV000200342.1,