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rs786205569

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205569(A;T)
Make rs786205569(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position71440650
GeneSLC4A4
is asnp
is mentioned by
dbSNPrs786205569
ebirs786205569
HLIrs786205569
Exacrs786205569
Varsomers786205569
Maprs786205569
PheGenIrs786205569
hapmaprs786205569
1000 genomesrs786205569
hgdprs786205569
ensemblrs786205569
gopubmedrs786205569
geneviewrs786205569
scholarrs786205569
googlers786205569
pharmgkbrs786205569
gwascentralrs786205569
openSNPrs786205569
23andMers786205569
23andMe allrs786205569
SNP Nexus

SNPshotrs786205569
SNPdbers786205569
MSV3drs786205569
GWAS Ctlgrs786205569
Max Magnitude0
ClinVar
Risk rs786205569(T;T)
Alt rs786205569(T;T)
Reference rs786205569(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC4A4
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.72306367A>T
CLNSRC
CLNACC RCV000171377.1,