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rs63749998

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63749998(C;C)
Make rs63749998(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position16163119
GeneABCC6
is asnp
is mentioned by
dbSNPrs63749998
ebirs63749998
HLIrs63749998
Exacrs63749998
Varsomers63749998
Maprs63749998
PheGenIrs63749998
hapmaprs63749998
1000 genomesrs63749998
hgdprs63749998
ensemblrs63749998
gopubmedrs63749998
geneviewrs63749998
scholarrs63749998
googlers63749998
pharmgkbrs63749998
gwascentralrs63749998
openSNPrs63749998
23andMers63749998
23andMe allrs63749998
SNP Nexus

SNPshotrs63749998
SNPdbers63749998
MSV3drs63749998
GWAS Ctlgrs63749998
Max Magnitude0
ClinVar
Risk rs63749998(C;C)
Alt rs63749998(C;C)
Reference rs63749998(T;T)
Significance Untested
Disease
Variation info
Gene ABCC6
CLNDBN
Reversed 1
HGVS NC_000016.9:g.16256976A>G
CLNSRC
CLNACC