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rs1057517995

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517995(A;A)
Make rs1057517995(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48134940
GeneMYEF2, SLC24A5
is asnp
is mentioned by
dbSNPrs1057517995
dbSNP (old)rs1057517995
ClinGenrs1057517995
ebirs1057517995
HLIrs1057517995
Exacrs1057517995
Gnomadrs1057517995
Varsomers1057517995
Maprs1057517995
PheGenIrs1057517995
Biobankrs1057517995
1000 genomesrs1057517995
hgdprs1057517995
ensemblrs1057517995
gopubmedrs1057517995
geneviewrs1057517995
scholarrs1057517995
googlers1057517995
pharmgkbrs1057517995
gwascentralrs1057517995
openSNPrs1057517995
23andMers1057517995
23andMe allrs1057517995
SNPshotrs1057517995
SNPdbers1057517995
MSV3drs1057517995
GWAS Ctlgrs1057517995
Max Magnitude0
ClinVar
Risk rs1057517995(A;A)
Alt rs1057517995(A;A)
Reference Rs1057517995(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC24A5
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48427137T>A
CLNSRC
CLNACC RCV000413130.1,