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rs532757890

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs532757890(A;A)
Make rs532757890(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position232484198
GeneECEL1
is asnp
is mentioned by
dbSNPrs532757890
dbSNP (old)rs532757890
ClinGenrs532757890
ebirs532757890
HLIrs532757890
Exacrs532757890
Gnomadrs532757890
Varsomers532757890
Maprs532757890
PheGenIrs532757890
Biobankrs532757890
1000 genomesrs532757890
hgdprs532757890
ensemblrs532757890
gopubmedrs532757890
geneviewrs532757890
scholarrs532757890
googlers532757890
pharmgkbrs532757890
gwascentralrs532757890
openSNPrs532757890
23andMers532757890
23andMe allrs532757890
SNP Nexus

SNPshotrs532757890
SNPdbers532757890
MSV3drs532757890
GWAS Ctlgrs532757890
Max Magnitude0
ClinVar
Risk rs532757890(A;A)
Alt rs532757890(A;A)
Reference Rs532757890(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ECEL1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.233348908G>A
CLNSRC UniProtKB (protein)
CLNACC RCV000171336.1,