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rs727503881

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503881(A;A)
Make rs727503881(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position102920365
GeneCOL11A1
is asnp
is mentioned by
dbSNPrs727503881
ebirs727503881
HLIrs727503881
Exacrs727503881
Varsomers727503881
Maprs727503881
PheGenIrs727503881
hapmaprs727503881
1000 genomesrs727503881
hgdprs727503881
ensemblrs727503881
gopubmedrs727503881
geneviewrs727503881
scholarrs727503881
googlers727503881
pharmgkbrs727503881
gwascentralrs727503881
openSNPrs727503881
23andMers727503881
23andMe allrs727503881
SNP Nexus

SNPshotrs727503881
SNPdbers727503881
MSV3drs727503881
GWAS Ctlgrs727503881
Max Magnitude0
ClinVar
Risk rs727503881(A;A)
Alt rs727503881(A;A)
Reference rs727503881(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene COL11A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.103385921C>T
CLNSRC
CLNACC RCV000153074.3,