rs863223903

Orientation

minus

Stabilized

minus

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

Make rs863223903(C;C)

Make rs863223903(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

55015610

Gene

ALAS2

is a	snp
is	mentioned by
dbSNP	rs863223903
dbSNP (classic)	rs863223903
ClinGen	rs863223903
ebi	rs863223903
HLI	rs863223903
Exac	rs863223903
Gnomad	rs863223903
Varsome	rs863223903
LitVar	rs863223903
Map	rs863223903
PheGenI	rs863223903
Biobank	rs863223903
1000 genomes	rs863223903
hgdp	rs863223903
ensembl	rs863223903
geneview	rs863223903
scholar	rs863223903
google	rs863223903
pharmgkb	rs863223903
gwascentral	rs863223903
openSNP	rs863223903
23andMe	rs863223903
SNPshot	rs863223903
SNPdbe	rs863223903
MSV3d	rs863223903
GWAS Ctlg	rs863223903

Max Magnitude

0

ClinVar
Risk	rs863223903(C;C)
Alt	rs863223903(C;C)
Reference	Rs863223903(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ALAS2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.55042043A>G
CLNSRC
CLNACC	RCV000197406.1,