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rs797044867

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044867(A;A)
Make rs797044867(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position110178196
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs797044867
ebirs797044867
HLIrs797044867
Exacrs797044867
Varsomers797044867
Maprs797044867
PheGenIrs797044867
hapmaprs797044867
1000 genomesrs797044867
hgdprs797044867
ensemblrs797044867
gopubmedrs797044867
geneviewrs797044867
scholarrs797044867
googlers797044867
pharmgkbrs797044867
gwascentralrs797044867
openSNPrs797044867
23andMers797044867
23andMe allrs797044867
SNP Nexus

SNPshotrs797044867
SNPdbers797044867
MSV3drs797044867
GWAS Ctlgrs797044867
Max Magnitude0
ClinVar
Risk rs797044867(A;A)
Alt rs797044867(A;A)
Reference rs797044867(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene COL4A1
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000013.10:g.110830543C>T
CLNSRC
CLNACC RCV000190674.1,