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rs1057518181

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518181(G;T)
Make rs1057518181(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position232486650
GeneECEL1
is asnp
is mentioned by
dbSNPrs1057518181
dbSNP (old)rs1057518181
ClinGenrs1057518181
ebirs1057518181
HLIrs1057518181
Exacrs1057518181
Gnomadrs1057518181
Varsomers1057518181
Maprs1057518181
PheGenIrs1057518181
Biobankrs1057518181
1000 genomesrs1057518181
hgdprs1057518181
ensemblrs1057518181
gopubmedrs1057518181
geneviewrs1057518181
scholarrs1057518181
googlers1057518181
pharmgkbrs1057518181
gwascentralrs1057518181
openSNPrs1057518181
23andMers1057518181
23andMe allrs1057518181
SNPshotrs1057518181
SNPdbers1057518181
MSV3drs1057518181
GWAS Ctlgrs1057518181
Max Magnitude0
ClinVar
Risk rs1057518181(T;T)
Alt rs1057518181(T;T)
Reference Rs1057518181(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ECEL1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.233351360C>A
CLNSRC
CLNACC RCV000414469.1,