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rs756771290

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs756771290(C;C)
Make rs756771290(C;T)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position215007788
GeneABCA12
is asnp
is mentioned by
dbSNPrs756771290
dbSNP (classic)rs756771290
ClinGenrs756771290
ebirs756771290
HLIrs756771290
Exacrs756771290
Gnomadrs756771290
Varsomers756771290
LitVarrs756771290
Maprs756771290
PheGenIrs756771290
Biobankrs756771290
1000 genomesrs756771290
hgdprs756771290
ensemblrs756771290
geneviewrs756771290
scholarrs756771290
googlers756771290
pharmgkbrs756771290
gwascentralrs756771290
openSNPrs756771290
23andMers756771290
23andMe allrs756771290
SNPshotrs756771290
SNPdbers756771290
MSV3drs756771290
GWAS Ctlgrs756771290
Max Magnitude0
ClinVar
Risk rs756771290(C;C)
Alt rs756771290(C;C)
Reference Rs756771290(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCA12
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.215872512T>C
CLNSRC
CLNACC RCV000255774.1,