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rs794727995

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727995(A;A)
Make rs794727995(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position160314111
GeneCOPA, NHLH1
is asnp
is mentioned by
dbSNPrs794727995
ebirs794727995
HLIrs794727995
Exacrs794727995
Varsomers794727995
Maprs794727995
PheGenIrs794727995
hapmaprs794727995
1000 genomesrs794727995
hgdprs794727995
ensemblrs794727995
gopubmedrs794727995
geneviewrs794727995
scholarrs794727995
googlers794727995
pharmgkbrs794727995
gwascentralrs794727995
openSNPrs794727995
23andMers794727995
23andMe allrs794727995
SNP Nexus

SNPshotrs794727995
SNPdbers794727995
MSV3drs794727995
GWAS Ctlgrs794727995
Max Magnitude0
ClinVar
Risk rs794727995(A;A)
Alt rs794727995(A;A)
Reference rs794727995(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.160283901C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000180778.3,