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rs483352841

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs483352841(C;G)
Make rs483352841(G;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position12884973
GeneKLF1
is asnp
is mentioned by
dbSNPrs483352841
ebirs483352841
HLIrs483352841
Exacrs483352841
Varsomers483352841
Maprs483352841
PheGenIrs483352841
hapmaprs483352841
1000 genomesrs483352841
hgdprs483352841
ensemblrs483352841
gopubmedrs483352841
geneviewrs483352841
scholarrs483352841
googlers483352841
pharmgkbrs483352841
gwascentralrs483352841
openSNPrs483352841
23andMers483352841
23andMe allrs483352841
SNP Nexus

SNPshotrs483352841
SNPdbers483352841
MSV3drs483352841
GWAS Ctlgrs483352841
Max Magnitude0
ClinVar
Risk rs483352841(G,T;G,T)
Alt rs483352841(G,T;G,T)
Reference rs483352841(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KLF1
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.12995787G>C
CLNSRC ClinVar
CLNACC RCV000087154.1,