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rs1057519599

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519599(C;T)
Make rs1057519599(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position155676622
GeneYY1AP1
is asnp
is mentioned by
dbSNPrs1057519599
dbSNP (old)rs1057519599
ClinGenrs1057519599
ebirs1057519599
HLIrs1057519599
Exacrs1057519599
Gnomadrs1057519599
Varsomers1057519599
LitVarrs1057519599
Maprs1057519599
PheGenIrs1057519599
Biobankrs1057519599
1000 genomesrs1057519599
hgdprs1057519599
ensemblrs1057519599
gopubmedrs1057519599
geneviewrs1057519599
scholarrs1057519599
googlers1057519599
pharmgkbrs1057519599
gwascentralrs1057519599
openSNPrs1057519599
23andMers1057519599
23andMe allrs1057519599
SNPshotrs1057519599
SNPdbers1057519599
MSV3drs1057519599
GWAS Ctlgrs1057519599
Max Magnitude0
ClinVar
Risk rs1057519599(T;T)
Alt rs1057519599(T;T)
Reference Rs1057519599(C;C)
Significance Pathogenic
Disease Grange syndrome
Variation info
Gene YY1AP1
CLNDBN Grange syndrome
Reversed 1
HGVS NC_000001.10:g.155646413G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000417120.1,