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rs1048457038

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position16421139
GeneISPD
is asnp
is mentioned by
dbSNPrs1048457038
dbSNP (old)rs1048457038
ClinGenrs1048457038
ebirs1048457038
HLIrs1048457038
Exacrs1048457038
Gnomadrs1048457038
Varsomers1048457038
Maprs1048457038
PheGenIrs1048457038
Biobankrs1048457038
1000 genomesrs1048457038
hgdprs1048457038
ensemblrs1048457038
gopubmedrs1048457038
geneviewrs1048457038
scholarrs1048457038
googlers1048457038
pharmgkbrs1048457038
gwascentralrs1048457038
openSNPrs1048457038
23andMers1048457038
23andMe allrs1048457038
SNPshotrs1048457038
SNPdbers1048457038
MSV3drs1048457038
GWAS Ctlgrs1048457038
Max Magnitude0
ClinVar
Risk rs1048457038(-;-)
Alt rs1048457038(-;-)
Reference Rs1048457038(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ISPD
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.16460764delC
CLNSRC
CLNACC RCV000484862.1,