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rs864309710

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309710(G;T)
Make rs864309710(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position160323447
GeneCOPA, NHLH1
is asnp
is mentioned by
dbSNPrs864309710
ebirs864309710
HLIrs864309710
Exacrs864309710
Varsomers864309710
Maprs864309710
PheGenIrs864309710
hapmaprs864309710
1000 genomesrs864309710
hgdprs864309710
ensemblrs864309710
gopubmedrs864309710
geneviewrs864309710
scholarrs864309710
googlers864309710
pharmgkbrs864309710
gwascentralrs864309710
openSNPrs864309710
23andMers864309710
23andMe allrs864309710
SNP Nexus

SNPshotrs864309710
SNPdbers864309710
MSV3drs864309710
GWAS Ctlgrs864309710
Max Magnitude0
ClinVar
Risk rs864309710(T;T)
Alt rs864309710(T;T)
Reference rs864309710(G;G)
Significance Pathogenic
Disease Autoimmune interstitial lung
Variation info
Gene COPA
CLNDBN Autoimmune interstitial lung, joint, and kidney disease
Reversed 1
HGVS NC_000001.10:g.160293237C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000203296.2,