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rs797044947

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044947(A;A)
Make rs797044947(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position110503855
GeneCOL4A2, COL4A2-AS1
is asnp
is mentioned by
dbSNPrs797044947
ebirs797044947
HLIrs797044947
Exacrs797044947
Varsomers797044947
Maprs797044947
PheGenIrs797044947
hapmaprs797044947
1000 genomesrs797044947
hgdprs797044947
ensemblrs797044947
gopubmedrs797044947
geneviewrs797044947
scholarrs797044947
googlers797044947
pharmgkbrs797044947
gwascentralrs797044947
openSNPrs797044947
23andMers797044947
23andMe allrs797044947
SNP Nexus

SNPshotrs797044947
SNPdbers797044947
MSV3drs797044947
GWAS Ctlgrs797044947
Max Magnitude0
ClinVar
Risk rs797044947(A;A)
Alt rs797044947(A;A)
Reference rs797044947(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene COL4A2-AS1 COL4A2
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000013.10:g.111156202G>A
CLNSRC
CLNACC RCV000190797.1,