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

rs886039329

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039329(A;A)
Make rs886039329(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position48567608
GeneCOL7A1
is asnp
is mentioned by
dbSNPrs886039329
dbSNP (classic)rs886039329
ClinGenrs886039329
ebirs886039329
HLIrs886039329
Exacrs886039329
Gnomadrs886039329
Varsomers886039329
LitVarrs886039329
Maprs886039329
PheGenIrs886039329
Biobankrs886039329
1000 genomesrs886039329
hgdprs886039329
ensemblrs886039329
geneviewrs886039329
scholarrs886039329
googlers886039329
pharmgkbrs886039329
gwascentralrs886039329
openSNPrs886039329
23andMers886039329
SNPshotrs886039329
SNPdbers886039329
MSV3drs886039329
GWAS Ctlgrs886039329
Max Magnitude0
ClinVar
Risk rs886039329(A;A)
Alt rs886039329(A;A)
Reference Rs886039329(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene COL7A1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.48605041C>T
CLNSRC
CLNACC RCV000254984.1,