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rs1057523629

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523629(A;A)
Make rs1057523629(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position7574253
GeneDSP
is asnp
is mentioned by
dbSNPrs1057523629
dbSNP (old)rs1057523629
ClinGenrs1057523629
ebirs1057523629
HLIrs1057523629
Exacrs1057523629
Gnomadrs1057523629
Varsomers1057523629
LitVarrs1057523629
Maprs1057523629
PheGenIrs1057523629
Biobankrs1057523629
1000 genomesrs1057523629
hgdprs1057523629
ensemblrs1057523629
gopubmedrs1057523629
geneviewrs1057523629
scholarrs1057523629
googlers1057523629
pharmgkbrs1057523629
gwascentralrs1057523629
openSNPrs1057523629
23andMers1057523629
23andMe allrs1057523629
SNPshotrs1057523629
SNPdbers1057523629
MSV3drs1057523629
GWAS Ctlgrs1057523629
Max Magnitude0
ClinVar
Risk rs1057523629(A;A)
Alt rs1057523629(A;A)
Reference Rs1057523629(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7574486G>A
CLNSRC
CLNACC RCV000441801.1,