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

rs1057520571

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520571(A;A)
Make rs1057520571(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position68218567
GeneCLN6
is asnp
is mentioned by
dbSNPrs1057520571
dbSNP (classic)rs1057520571
ClinGenrs1057520571
ebirs1057520571
HLIrs1057520571
Exacrs1057520571
Gnomadrs1057520571
Varsomers1057520571
LitVarrs1057520571
Maprs1057520571
PheGenIrs1057520571
Biobankrs1057520571
1000 genomesrs1057520571
hgdprs1057520571
ensemblrs1057520571
geneviewrs1057520571
scholarrs1057520571
googlers1057520571
pharmgkbrs1057520571
gwascentralrs1057520571
openSNPrs1057520571
23andMers1057520571
SNPshotrs1057520571
SNPdbers1057520571
MSV3drs1057520571
GWAS Ctlgrs1057520571
Max Magnitude0
ClinVar
Risk rs1057520571(A;A)
Alt rs1057520571(A;A)
Reference Rs1057520571(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CLN6
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.68510905C>T
CLNSRC
CLNACC RCV000420815.1,