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rs886039720

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039720(A;A)
Make rs886039720(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position48579376
GeneCOL7A1, MIR711
is asnp
is mentioned by
dbSNPrs886039720
dbSNP (classic)rs886039720
ClinGenrs886039720
ebirs886039720
HLIrs886039720
Exacrs886039720
Gnomadrs886039720
Varsomers886039720
LitVarrs886039720
Maprs886039720
PheGenIrs886039720
Biobankrs886039720
1000 genomesrs886039720
hgdprs886039720
ensemblrs886039720
geneviewrs886039720
scholarrs886039720
googlers886039720
pharmgkbrs886039720
gwascentralrs886039720
openSNPrs886039720
23andMers886039720
SNPshotrs886039720
SNPdbers886039720
MSV3drs886039720
GWAS Ctlgrs886039720
Max Magnitude0
ClinVar
Risk rs886039720(A;A)
Alt rs886039720(A;A)
Reference Rs886039720(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MIR711 COL7A1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.48616809C>T
CLNSRC
CLNACC RCV000255538.1,