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rs866061439

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs866061439(C;T)
Make rs866061439(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position48575233
GeneCOL7A1
is asnp
is mentioned by
dbSNPrs866061439
dbSNP (classic)rs866061439
ClinGenrs866061439
ebirs866061439
HLIrs866061439
Exacrs866061439
Gnomadrs866061439
Varsomers866061439
LitVarrs866061439
Maprs866061439
PheGenIrs866061439
Biobankrs866061439
1000 genomesrs866061439
hgdprs866061439
ensemblrs866061439
geneviewrs866061439
scholarrs866061439
googlers866061439
pharmgkbrs866061439
gwascentralrs866061439
openSNPrs866061439
23andMers866061439
SNPshotrs866061439
SNPdbers866061439
MSV3drs866061439
GWAS Ctlgrs866061439
Max Magnitude0
ClinVar
Risk rs866061439(T;T)
Alt rs866061439(T;T)
Reference Rs866061439(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene COL7A1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.48612666C>T
CLNSRC
CLNACC RCV000373392.1,