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

rs1057517899

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517899(C;T)
Make rs1057517899(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position5711552
GeneEVC
is asnp
is mentioned by
dbSNPrs1057517899
dbSNP (classic)rs1057517899
ClinGenrs1057517899
ebirs1057517899
HLIrs1057517899
Exacrs1057517899
Gnomadrs1057517899
Varsomers1057517899
LitVarrs1057517899
Maprs1057517899
PheGenIrs1057517899
Biobankrs1057517899
1000 genomesrs1057517899
hgdprs1057517899
ensemblrs1057517899
geneviewrs1057517899
scholarrs1057517899
googlers1057517899
pharmgkbrs1057517899
gwascentralrs1057517899
openSNPrs1057517899
23andMers1057517899
23andMe allrs1057517899
SNPshotrs1057517899
SNPdbers1057517899
MSV3drs1057517899
GWAS Ctlgrs1057517899
Max Magnitude0
ClinVar
Risk rs1057517899(T;T)
Alt rs1057517899(T;T)
Reference Rs1057517899(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EVC
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.5713279C>T
CLNSRC
CLNACC RCV000413234.1,