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

rs1057517875

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs1057517875(-;-)
Make rs1057517875(-;CT)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position5748244
GeneEVC
is asnp
is mentioned by
dbSNPrs1057517875
dbSNP (old)rs1057517875
ClinGenrs1057517875
ebirs1057517875
HLIrs1057517875
Exacrs1057517875
Gnomadrs1057517875
Varsomers1057517875
Maprs1057517875
PheGenIrs1057517875
Biobankrs1057517875
1000 genomesrs1057517875
hgdprs1057517875
ensemblrs1057517875
gopubmedrs1057517875
geneviewrs1057517875
scholarrs1057517875
googlers1057517875
pharmgkbrs1057517875
gwascentralrs1057517875
openSNPrs1057517875
23andMers1057517875
23andMe allrs1057517875
SNPshotrs1057517875
SNPdbers1057517875
MSV3drs1057517875
GWAS Ctlgrs1057517875
Max Magnitude0
ClinVar
Risk rs1057517875(-;-)
Alt rs1057517875(-;-)
Reference Rs1057517875(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene EVC
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.5749971_5749972delCT
CLNSRC
CLNACC RCV000414675.1,