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rs63749807

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63749807(G;T)
Make rs63749807(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position16163102
GeneABCC6
is asnp
is mentioned by
dbSNPrs63749807
ebirs63749807
HLIrs63749807
Exacrs63749807
Varsomers63749807
Maprs63749807
PheGenIrs63749807
hapmaprs63749807
1000 genomesrs63749807
hgdprs63749807
ensemblrs63749807
gopubmedrs63749807
geneviewrs63749807
scholarrs63749807
googlers63749807
pharmgkbrs63749807
gwascentralrs63749807
openSNPrs63749807
23andMers63749807
23andMe allrs63749807
SNP Nexus

SNPshotrs63749807
SNPdbers63749807
MSV3drs63749807
GWAS Ctlgrs63749807
Max Magnitude0
ClinVar
Risk rs63749807(T;T)
Alt rs63749807(T;T)
Reference rs63749807(G;G)
Significance Untested
Disease
Variation info
Gene ABCC6
CLNDBN
Reversed 1
HGVS NC_000016.9:g.16256959C>A
CLNSRC
CLNACC