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

rs1057519598

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519598(G;T)
Make rs1057519598(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position155659923
GeneYY1AP1
is asnp
is mentioned by
dbSNPrs1057519598
dbSNP (old)rs1057519598
ClinGenrs1057519598
ebirs1057519598
HLIrs1057519598
Exacrs1057519598
Gnomadrs1057519598
Varsomers1057519598
Maprs1057519598
PheGenIrs1057519598
Biobankrs1057519598
1000 genomesrs1057519598
hgdprs1057519598
ensemblrs1057519598
gopubmedrs1057519598
geneviewrs1057519598
scholarrs1057519598
googlers1057519598
pharmgkbrs1057519598
gwascentralrs1057519598
openSNPrs1057519598
23andMers1057519598
23andMe allrs1057519598
SNPshotrs1057519598
SNPdbers1057519598
MSV3drs1057519598
GWAS Ctlgrs1057519598
Max Magnitude0
ClinVar
Risk rs1057519598(T;T)
Alt rs1057519598(T;T)
Reference Rs1057519598(G;G)
Significance Pathogenic
Disease Grange syndrome
Variation info
Gene YY1AP1
CLNDBN Grange syndrome
Reversed 1
HGVS NC_000001.10:g.155629714C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000417123.1,