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rs780389591

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs780389591(A;A)
Make rs780389591(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position219570282
GeneINHA, OBSL1
is asnp
is mentioned by
dbSNPrs780389591
ebirs780389591
HLIrs780389591
Exacrs780389591
Varsomers780389591
Maprs780389591
PheGenIrs780389591
hapmaprs780389591
1000 genomesrs780389591
hgdprs780389591
ensemblrs780389591
gopubmedrs780389591
geneviewrs780389591
scholarrs780389591
googlers780389591
pharmgkbrs780389591
gwascentralrs780389591
openSNPrs780389591
23andMers780389591
23andMe allrs780389591
SNP Nexus

SNPshotrs780389591
SNPdbers780389591
MSV3drs780389591
GWAS Ctlgrs780389591
Max Magnitude0
ClinVar
Risk rs780389591(A;A)
Alt rs780389591(A;A)
Reference rs780389591(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OBSL1 INHA
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.220435004G>T
CLNSRC
CLNACC RCV000171333.1,