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rs368529673

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368529673(C;T)
Make rs368529673(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position48568100
GeneCOL7A1
is asnp
is mentioned by
dbSNPrs368529673
dbSNP (classic)rs368529673
ClinGenrs368529673
ebirs368529673
HLIrs368529673
Exacrs368529673
Gnomadrs368529673
Varsomers368529673
LitVarrs368529673
Maprs368529673
PheGenIrs368529673
Biobankrs368529673
1000 genomesrs368529673
hgdprs368529673
ensemblrs368529673
geneviewrs368529673
scholarrs368529673
googlers368529673
pharmgkbrs368529673
gwascentralrs368529673
openSNPrs368529673
23andMers368529673
SNPshotrs368529673
SNPdbers368529673
MSV3drs368529673
GWAS Ctlgrs368529673
Max Magnitude0
ClinVar
Risk rs368529673(T;T)
Alt rs368529673(T;T)
Reference Rs368529673(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene COL7A1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.48605533C>T
CLNSRC
CLNACC RCV000255882.1,