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rs121909577

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909577(C;C)
Make rs121909577(C;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position85328586
GeneCA1
is asnp
is mentioned by
dbSNPrs121909577
ebirs121909577
HLIrs121909577
Exacrs121909577
Varsomers121909577
Maprs121909577
PheGenIrs121909577
hapmaprs121909577
1000 genomesrs121909577
hgdprs121909577
ensemblrs121909577
gopubmedrs121909577
geneviewrs121909577
scholarrs121909577
googlers121909577
pharmgkbrs121909577
gwascentralrs121909577
openSNPrs121909577
23andMers121909577
23andMe allrs121909577
SNP Nexus

SNPshotrs121909577
SNPdbers121909577
MSV3drs121909577
GWAS Ctlgrs121909577
Max Magnitude0
OMIM114800
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909577(C;C)
Alt rs121909577(C;C)
Reference rs121909577(G;G)
Significance Pathogenic
Disease Carbonic anhydrase I
Variation info
Gene CA1
CLNDBN Carbonic anhydrase I, Guam
Reversed 1
HGVS NC_000008.10:g.86240815C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019171.23,