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

rs1057520568

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520568(C;C)
Make rs1057520568(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position48579385
GeneCOL7A1, MIR711
is asnp
is mentioned by
dbSNPrs1057520568
dbSNP (classic)rs1057520568
ClinGenrs1057520568
ebirs1057520568
HLIrs1057520568
Exacrs1057520568
Gnomadrs1057520568
Varsomers1057520568
LitVarrs1057520568
Maprs1057520568
PheGenIrs1057520568
Biobankrs1057520568
1000 genomesrs1057520568
hgdprs1057520568
ensemblrs1057520568
geneviewrs1057520568
scholarrs1057520568
googlers1057520568
pharmgkbrs1057520568
gwascentralrs1057520568
openSNPrs1057520568
23andMers1057520568
SNPshotrs1057520568
SNPdbers1057520568
MSV3drs1057520568
GWAS Ctlgrs1057520568
Max Magnitude0
ClinVar
Risk rs1057520568(C;C)
Alt rs1057520568(C;C)
Reference Rs1057520568(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MIR711 COL7A1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.48616818C>G
CLNSRC
CLNACC RCV000424969.1,