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rs1057518101

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518101(G;T)
Make rs1057518101(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position7584202
GeneDSP
is asnp
is mentioned by
dbSNPrs1057518101
dbSNP (old)rs1057518101
ClinGenrs1057518101
ebirs1057518101
HLIrs1057518101
Exacrs1057518101
Gnomadrs1057518101
Varsomers1057518101
Maprs1057518101
PheGenIrs1057518101
Biobankrs1057518101
1000 genomesrs1057518101
hgdprs1057518101
ensemblrs1057518101
gopubmedrs1057518101
geneviewrs1057518101
scholarrs1057518101
googlers1057518101
pharmgkbrs1057518101
gwascentralrs1057518101
openSNPrs1057518101
23andMers1057518101
23andMe allrs1057518101
SNPshotrs1057518101
SNPdbers1057518101
MSV3drs1057518101
GWAS Ctlgrs1057518101
Max Magnitude0
ClinVar
Risk rs1057518101(T;T)
Alt rs1057518101(T;T)
Reference Rs1057518101(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7584435G>T
CLNSRC
CLNACC RCV000413488.1,