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rs141026028

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141026028(A;A)
Make rs141026028(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7583758
GeneDSP
is asnp
is mentioned by
dbSNPrs141026028
ebirs141026028
HLIrs141026028
Exacrs141026028
Varsomers141026028
Maprs141026028
PheGenIrs141026028
hapmaprs141026028
1000 genomesrs141026028
hgdprs141026028
ensemblrs141026028
gopubmedrs141026028
geneviewrs141026028
scholarrs141026028
googlers141026028
pharmgkbrs141026028
gwascentralrs141026028
openSNPrs141026028
23andMers141026028
23andMe allrs141026028
SNP Nexus

SNPshotrs141026028
SNPdbers141026028
MSV3drs141026028
GWAS Ctlgrs141026028
Max Magnitude0
ClinVar
Risk rs141026028(A;A)
Alt rs141026028(A;A)
Reference rs141026028(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7583991C>T
CLNSRC
CLNACC RCV000181342.2,