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rs794727993

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727993(A;A)
Make rs794727993(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position160323439
GeneCOPA, NHLH1
is asnp
is mentioned by
dbSNPrs794727993
ebirs794727993
HLIrs794727993
Exacrs794727993
Varsomers794727993
Maprs794727993
PheGenIrs794727993
hapmaprs794727993
1000 genomesrs794727993
hgdprs794727993
ensemblrs794727993
gopubmedrs794727993
geneviewrs794727993
scholarrs794727993
googlers794727993
pharmgkbrs794727993
gwascentralrs794727993
openSNPrs794727993
23andMers794727993
23andMe allrs794727993
SNP Nexus

SNPshotrs794727993
SNPdbers794727993
MSV3drs794727993
GWAS Ctlgrs794727993
Max Magnitude0
ClinVar
Risk rs794727993(A;A)
Alt rs794727993(A;A)
Reference rs794727993(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.160293229C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000180776.3,