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rs1057519597

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519597(A;A)
Make rs1057519597(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position155659934
GeneYY1AP1
is asnp
is mentioned by
dbSNPrs1057519597
dbSNP (old)rs1057519597
ClinGenrs1057519597
ebirs1057519597
HLIrs1057519597
Exacrs1057519597
Gnomadrs1057519597
Varsomers1057519597
Maprs1057519597
PheGenIrs1057519597
Biobankrs1057519597
1000 genomesrs1057519597
hgdprs1057519597
ensemblrs1057519597
gopubmedrs1057519597
geneviewrs1057519597
scholarrs1057519597
googlers1057519597
pharmgkbrs1057519597
gwascentralrs1057519597
openSNPrs1057519597
23andMers1057519597
23andMe allrs1057519597
SNPshotrs1057519597
SNPdbers1057519597
MSV3drs1057519597
GWAS Ctlgrs1057519597
Max Magnitude0
ClinVar
Risk rs1057519597(A;A) rs1057519597(G;G)
Alt rs1057519597(A;A) rs1057519597(G;G)
Reference Rs1057519597(T;T)
Significance Pathogenic
Disease Grange syndrome
Variation info
Gene YY1AP1
CLNDBN Grange syndrome
Reversed 1
HGVS NC_000001.10:g.155629725A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000417119.1,