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rs786205561

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205561(C;C)
Make rs786205561(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position48581295
GeneCOL7A1
is asnp
is mentioned by
dbSNPrs786205561
ebirs786205561
HLIrs786205561
Exacrs786205561
Varsomers786205561
Maprs786205561
PheGenIrs786205561
hapmaprs786205561
1000 genomesrs786205561
hgdprs786205561
ensemblrs786205561
gopubmedrs786205561
geneviewrs786205561
scholarrs786205561
googlers786205561
pharmgkbrs786205561
gwascentralrs786205561
openSNPrs786205561
23andMers786205561
23andMe allrs786205561
SNP Nexus

SNPshotrs786205561
SNPdbers786205561
MSV3drs786205561
GWAS Ctlgrs786205561
Max Magnitude0
ClinVar
Risk rs786205561(C;C)
Alt rs786205561(C;C)
Reference rs786205561(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL7A1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.48618728C>G
CLNSRC
CLNACC RCV000171361.1,