Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057524848

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524848(A;A)
Make rs1057524848(A;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position154380772
GeneEMD
is asnp
is mentioned by
dbSNPrs1057524848
dbSNP (old)rs1057524848
ClinGenrs1057524848
ebirs1057524848
HLIrs1057524848
Exacrs1057524848
Gnomadrs1057524848
Varsomers1057524848
Maprs1057524848
PheGenIrs1057524848
Biobankrs1057524848
1000 genomesrs1057524848
hgdprs1057524848
ensemblrs1057524848
gopubmedrs1057524848
geneviewrs1057524848
scholarrs1057524848
googlers1057524848
pharmgkbrs1057524848
gwascentralrs1057524848
openSNPrs1057524848
23andMers1057524848
23andMe allrs1057524848
SNPshotrs1057524848
SNPdbers1057524848
MSV3drs1057524848
GWAS Ctlgrs1057524848
Max Magnitude0
ClinVar
Risk rs1057524848(A;A)
Alt rs1057524848(A;A)
Reference Rs1057524848(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene EMD
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.153609132T>A
CLNSRC
CLNACC RCV000441327.1,