Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057522832

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057522832(C;C)
Make rs1057522832(C;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position55015586
GeneALAS2
is asnp
is mentioned by
dbSNPrs1057522832
dbSNP (old)rs1057522832
ClinGenrs1057522832
ebirs1057522832
HLIrs1057522832
Exacrs1057522832
Gnomadrs1057522832
Varsomers1057522832
LitVarrs1057522832
Maprs1057522832
PheGenIrs1057522832
Biobankrs1057522832
1000 genomesrs1057522832
hgdprs1057522832
ensemblrs1057522832
gopubmedrs1057522832
geneviewrs1057522832
scholarrs1057522832
googlers1057522832
pharmgkbrs1057522832
gwascentralrs1057522832
openSNPrs1057522832
23andMers1057522832
23andMe allrs1057522832
SNPshotrs1057522832
SNPdbers1057522832
MSV3drs1057522832
GWAS Ctlgrs1057522832
Max Magnitude0
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,