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rs111929073

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111929073(A;A)
Make rs111929073(A;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position188999471
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs111929073
ebirs111929073
HLIrs111929073
Exacrs111929073
Varsomers111929073
Maprs111929073
PheGenIrs111929073
hapmaprs111929073
1000 genomesrs111929073
hgdprs111929073
ensemblrs111929073
gopubmedrs111929073
geneviewrs111929073
scholarrs111929073
googlers111929073
pharmgkbrs111929073
gwascentralrs111929073
openSNPrs111929073
23andMers111929073
23andMe allrs111929073
SNP Nexus

SNPshotrs111929073
SNPdbers111929073
MSV3drs111929073
GWAS Ctlgrs111929073
Max Magnitude0
ClinVar
Risk rs111929073(A,T;A,T)
Alt rs111929073(A,T;A,T)
Reference rs111929073(G;G)
Significance Other
Disease Ehlers-Danlos syndrome
Variation info
Gene COL3A1
CLNDBN Ehlers-Danlos syndrome, type 4
Reversed 0
HGVS NC_000002.11:g.189864197G>T
CLNSRC Ehlers-Danlos Syndrome Variant Database COL3A1
CLNACC RCV000087633.2,