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rs878853002

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853002(A;A)
Make rs878853002(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position44255272
GeneSLC4A1
is asnp
is mentioned by
dbSNPrs878853002
ebirs878853002
HLIrs878853002
Exacrs878853002
Varsomers878853002
Maprs878853002
PheGenIrs878853002
hapmaprs878853002
1000 genomesrs878853002
hgdprs878853002
ensemblrs878853002
gopubmedrs878853002
geneviewrs878853002
scholarrs878853002
googlers878853002
pharmgkbrs878853002
gwascentralrs878853002
openSNPrs878853002
23andMers878853002
23andMe allrs878853002
SNP Nexus

SNPshotrs878853002
SNPdbers878853002
MSV3drs878853002
GWAS Ctlgrs878853002
Max Magnitude0
ClinVar
Risk rs878853002(A;A)
Alt rs878853002(A;A)
Reference rs878853002(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC4A1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.42332640C>T
CLNSRC
CLNACC RCV000224119.1,