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rs727502784

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727502784(A;G)
Make rs727502784(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position38916306
GeneCCER2, SARS2
is asnp
is mentioned by
dbSNPrs727502784
ebirs727502784
HLIrs727502784
Exacrs727502784
Varsomers727502784
Maprs727502784
PheGenIrs727502784
hapmaprs727502784
1000 genomesrs727502784
hgdprs727502784
ensemblrs727502784
gopubmedrs727502784
geneviewrs727502784
scholarrs727502784
googlers727502784
pharmgkbrs727502784
gwascentralrs727502784
openSNPrs727502784
23andMers727502784
23andMe allrs727502784
SNP Nexus

SNPshotrs727502784
SNPdbers727502784
MSV3drs727502784
GWAS Ctlgrs727502784
Max Magnitude0
ClinVar
Risk rs727502784(G;G)
Alt rs727502784(G;G)
Reference rs727502784(A;A)
Significance Pathogenic
Disease Hyperuricemia
Variation info
Gene SARS2
CLNDBN Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis
Reversed 1
HGVS NC_000019.9:g.39406946T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023973.4,