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rs67729041

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs67729041(A;A)
Make rs67729041(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position94409778
GeneCOL1A2
is asnp
is mentioned by
dbSNPrs67729041
dbSNP (classic)rs67729041
ClinGenrs67729041
ebirs67729041
HLIrs67729041
Exacrs67729041
Gnomadrs67729041
Varsomers67729041
LitVarrs67729041
Maprs67729041
PheGenIrs67729041
Biobankrs67729041
1000 genomesrs67729041
hgdprs67729041
ensemblrs67729041
geneviewrs67729041
scholarrs67729041
googlers67729041
pharmgkbrs67729041
gwascentralrs67729041
openSNPrs67729041
23andMers67729041
SNPshotrs67729041
SNPdbers67729041
MSV3drs67729041
GWAS Ctlgrs67729041
Max Magnitude0
ClinVar
Risk rs67729041(A;A) rs67729041(T;T)
Alt rs67729041(A;A) rs67729041(T;T)
Reference Rs67729041(G;G)
Significance Pathogenic
Disease Osteogenesis imperfecta type III
Variation info
Gene COL1A2
CLNDBN Osteogenesis imperfecta type III
Reversed 0
HGVS NC_000007.13:g.94039090G>A
CLNSRC
CLNACC RCV000490716.1,