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

rs1057517706

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(TTTG;TTTG) 0 common in clinvar
Make rs1057517706(-;-)
Make rs1057517706(-;TTGT)
Make rs1057517706(TTGT;TTGT)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position130997737
GeneATP2C1
is asnp
is mentioned by
dbSNPrs1057517706
dbSNP (old)rs1057517706
ClinGenrs1057517706
ebirs1057517706
HLIrs1057517706
Exacrs1057517706
Gnomadrs1057517706
Varsomers1057517706
Maprs1057517706
PheGenIrs1057517706
Biobankrs1057517706
1000 genomesrs1057517706
hgdprs1057517706
ensemblrs1057517706
gopubmedrs1057517706
geneviewrs1057517706
scholarrs1057517706
googlers1057517706
pharmgkbrs1057517706
gwascentralrs1057517706
openSNPrs1057517706
23andMers1057517706
23andMe allrs1057517706
SNPshotrs1057517706
SNPdbers1057517706
MSV3drs1057517706
GWAS Ctlgrs1057517706
Max Magnitude0
ClinVar
Risk rs1057517706(-;-)
Alt rs1057517706(-;-)
Reference Rs1057517706(TTTG;TTTG)
Significance Pathogenic
Disease not provided
Variation info
Gene ATP2C1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.130716581_130716584delTTGT
CLNSRC
CLNACC RCV000412997.1,