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rs63750135

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750135(C;T)
Make rs63750135(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position16150197
GeneABCC6
is asnp
is mentioned by
dbSNPrs63750135
dbSNP (classic)rs63750135
ClinGenrs63750135
ebirs63750135
HLIrs63750135
Exacrs63750135
Gnomadrs63750135
Varsomers63750135
LitVarrs63750135
Maprs63750135
PheGenIrs63750135
Biobankrs63750135
1000 genomesrs63750135
hgdprs63750135
ensemblrs63750135
geneviewrs63750135
scholarrs63750135
googlers63750135
pharmgkbrs63750135
gwascentralrs63750135
openSNPrs63750135
23andMers63750135
SNPshotrs63750135
SNPdbers63750135
MSV3drs63750135
GWAS Ctlgrs63750135
Max Magnitude0
ClinVar
Risk rs63750135(T;T)
Alt rs63750135(T;T)
Reference Rs63750135(C;C)
Significance Untested
Disease
Variation info
Gene ABCC6
CLNDBN
Reversed 1
HGVS NC_000016.9:g.16244054G>A
CLNSRC
CLNACC