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

rs1057518623

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518623(-;-)
Make rs1057518623(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position117835443
GeneEXT1
is asnp
is mentioned by
dbSNPrs1057518623
dbSNP (old)rs1057518623
ClinGenrs1057518623
ebirs1057518623
HLIrs1057518623
Exacrs1057518623
Gnomadrs1057518623
Varsomers1057518623
Maprs1057518623
PheGenIrs1057518623
Biobankrs1057518623
1000 genomesrs1057518623
hgdprs1057518623
ensemblrs1057518623
gopubmedrs1057518623
geneviewrs1057518623
scholarrs1057518623
googlers1057518623
pharmgkbrs1057518623
gwascentralrs1057518623
openSNPrs1057518623
23andMers1057518623
23andMe allrs1057518623
SNPshotrs1057518623
SNPdbers1057518623
MSV3drs1057518623
GWAS Ctlgrs1057518623
Max Magnitude0
ClinVar
Risk rs1057518623(-;-)
Alt rs1057518623(-;-)
Reference Rs1057518623(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EXT1
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.118847682delC
CLNSRC
CLNACC RCV000413669.1,