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rs201766106

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201766106(A;A)
Make rs201766106(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position16214428
GeneABCC6, LOC105371100
is asnp
is mentioned by
dbSNPrs201766106
dbSNP (classic)rs201766106
ClinGenrs201766106
ebirs201766106
HLIrs201766106
Exacrs201766106
Gnomadrs201766106
Varsomers201766106
LitVarrs201766106
Maprs201766106
PheGenIrs201766106
Biobankrs201766106
1000 genomesrs201766106
hgdprs201766106
ensemblrs201766106
geneviewrs201766106
scholarrs201766106
googlers201766106
pharmgkbrs201766106
gwascentralrs201766106
openSNPrs201766106
23andMers201766106
SNPshotrs201766106
SNPdbers201766106
MSV3drs201766106
GWAS Ctlgrs201766106
Max Magnitude0
ClinVar
Risk rs201766106(A;A)
Alt rs201766106(A;A)
Reference Rs201766106(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCC6
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.16308285G>A
CLNSRC
CLNACC RCV000413335.1,