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rs41278172

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41278172(A;A)
Make rs41278172(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position16161567
GeneABCC6
is asnp
is mentioned by
dbSNPrs41278172
ebirs41278172
HLIrs41278172
Exacrs41278172
Varsomers41278172
Maprs41278172
PheGenIrs41278172
hapmaprs41278172
1000 genomesrs41278172
hgdprs41278172
ensemblrs41278172
gopubmedrs41278172
geneviewrs41278172
scholarrs41278172
googlers41278172
pharmgkbrs41278172
gwascentralrs41278172
openSNPrs41278172
23andMers41278172
23andMe allrs41278172
SNP Nexus

SNPshotrs41278172
SNPdbers41278172
MSV3drs41278172
GWAS Ctlgrs41278172
GMAF0.0124
Max Magnitude0
ClinVar
Risk rs41278172(A;A)
Alt rs41278172(A;A)
Reference rs41278172(G;G)
Significance Untested
Disease
Variation info
Gene ABCC6
CLNDBN
Reversed 0
HGVS NC_000016.9:g.16255424G>A
CLNSRC
CLNACC