Have questions? Visit https://www.reddit.com/r/SNPedia

rs11861980

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11861980(A;A)
Make rs11861980(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position16173376
GeneABCC6
is asnp
is mentioned by
dbSNPrs11861980
ebirs11861980
HLIrs11861980
Exacrs11861980
Varsomers11861980
Maprs11861980
PheGenIrs11861980
hapmaprs11861980
1000 genomesrs11861980
hgdprs11861980
ensemblrs11861980
gopubmedrs11861980
geneviewrs11861980
scholarrs11861980
googlers11861980
pharmgkbrs11861980
gwascentralrs11861980
openSNPrs11861980
23andMers11861980
23andMe allrs11861980
SNP Nexus

SNPshotrs11861980
SNPdbers11861980
MSV3drs11861980
GWAS Ctlgrs11861980
GMAF0.003214
Max Magnitude0
ClinVar
Risk rs11861980(A,C;A,C)
Alt rs11861980(A,C;A,C)
Reference rs11861980(G;G)
Significance Untested
Disease
Variation info
Gene ABCC6
CLNDBN
Reversed 0
HGVS NC_000016.9:g.16267233G>C
CLNSRC
CLNACC


? (C;C) (C;G) (G;G) 28
OMIM264800
Desc
Variant
Relatedalso


GET Evidence
ABCC6-R899C
aa_change Arg899Cys
aa_change_short R899C
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.00148726
summary