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rs199974259

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199974259(G;T)
Make rs199974259(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position56902509
GeneMIR6863, SLC12A3
is asnp
is mentioned by
dbSNPrs199974259
dbSNP (old)rs199974259
ClinGenrs199974259
ebirs199974259
HLIrs199974259
Exacrs199974259
Gnomadrs199974259
Varsomers199974259
LitVarrs199974259
Maprs199974259
PheGenIrs199974259
Biobankrs199974259
1000 genomesrs199974259
hgdprs199974259
ensemblrs199974259
gopubmedrs199974259
geneviewrs199974259
scholarrs199974259
googlers199974259
pharmgkbrs199974259
gwascentralrs199974259
openSNPrs199974259
23andMers199974259
23andMe allrs199974259
SNPshotrs199974259
SNPdbers199974259
MSV3drs199974259
GWAS Ctlgrs199974259
Max Magnitude0
ClinVar
Risk rs199974259(T;T)
Alt rs199974259(T;T)
Reference Rs199974259(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC12A3 MIR6863
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.56936421G>T
CLNSRC
CLNACC RCV000412851.1,