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rs149701627

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs149701627(C;T)
Make rs149701627(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7565469
GeneDSP
is asnp
is mentioned by
dbSNPrs149701627
ebirs149701627
HLIrs149701627
Exacrs149701627
Varsomers149701627
Maprs149701627
PheGenIrs149701627
hapmaprs149701627
1000 genomesrs149701627
hgdprs149701627
ensemblrs149701627
gopubmedrs149701627
geneviewrs149701627
scholarrs149701627
googlers149701627
pharmgkbrs149701627
gwascentralrs149701627
openSNPrs149701627
23andMers149701627
23andMe allrs149701627
SNP Nexus

SNPshotrs149701627
SNPdbers149701627
MSV3drs149701627
GWAS Ctlgrs149701627
Max Magnitude0
ClinVar
Risk rs149701627(T;T)
Alt rs149701627(T;T)
Reference rs149701627(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7565702C>G
CLNSRC
CLNACC RCV000181280.1,