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rs769752636

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 5.5 Ehlers-Danlos Syndrome (EDS) classic type
Make rs769752636(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position134730386
GeneCOL5A1
is asnp
is mentioned by
dbSNPrs769752636
dbSNP (classic)rs769752636
ClinGenrs769752636
ebirs769752636
HLIrs769752636
Exacrs769752636
Gnomadrs769752636
Varsomers769752636
LitVarrs769752636
Maprs769752636
PheGenIrs769752636
Biobankrs769752636
1000 genomesrs769752636
hgdprs769752636
ensemblrs769752636
geneviewrs769752636
scholarrs769752636
googlers769752636
pharmgkbrs769752636
gwascentralrs769752636
openSNPrs769752636
23andMers769752636
SNPshotrs769752636
SNPdbers769752636
MSV3drs769752636
GWAS Ctlgrs769752636
Max Magnitude5.5
ClinVar
Risk rs769752636(A;A) rs769752636(T;T)
Alt rs769752636(A;A) rs769752636(T;T)
Reference Rs769752636(G;G)
Significance Pathogenic
Disease Ehlers-Danlos syndrome
Variation info
Gene COL5A1
CLNDBN Ehlers-Danlos syndrome, classic type
Reversed 0
HGVS NC_000009.11:g.137622232G>T
CLNSRC
CLNACC RCV000467841.1,