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

rs1057518242

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518242(-;-)
Make rs1057518242(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position122934664
GeneSPATA5
is asnp
is mentioned by
dbSNPrs1057518242
dbSNP (old)rs1057518242
ClinGenrs1057518242
ebirs1057518242
HLIrs1057518242
Exacrs1057518242
Gnomadrs1057518242
Varsomers1057518242
Maprs1057518242
PheGenIrs1057518242
Biobankrs1057518242
1000 genomesrs1057518242
hgdprs1057518242
ensemblrs1057518242
gopubmedrs1057518242
geneviewrs1057518242
scholarrs1057518242
googlers1057518242
pharmgkbrs1057518242
gwascentralrs1057518242
openSNPrs1057518242
23andMers1057518242
23andMe allrs1057518242
SNPshotrs1057518242
SNPdbers1057518242
MSV3drs1057518242
GWAS Ctlgrs1057518242
Max Magnitude0
ClinVar
Risk rs1057518242(-;-)
Alt rs1057518242(-;-)
Reference Rs1057518242(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPATA5
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.123855819delT
CLNSRC
CLNACC RCV000413360.1,