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rs1057521096

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521096(A;A)
Make rs1057521096(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position69964897
GeneMITF
is asnp
is mentioned by
dbSNPrs1057521096
dbSNP (old)rs1057521096
ClinGenrs1057521096
ebirs1057521096
HLIrs1057521096
Exacrs1057521096
Gnomadrs1057521096
Varsomers1057521096
Maprs1057521096
PheGenIrs1057521096
Biobankrs1057521096
1000 genomesrs1057521096
hgdprs1057521096
ensemblrs1057521096
gopubmedrs1057521096
geneviewrs1057521096
scholarrs1057521096
googlers1057521096
pharmgkbrs1057521096
gwascentralrs1057521096
openSNPrs1057521096
23andMers1057521096
23andMe allrs1057521096
SNPshotrs1057521096
SNPdbers1057521096
MSV3drs1057521096
GWAS Ctlgrs1057521096
Max Magnitude0
ClinVar
Risk rs1057521096(A;A)
Alt rs1057521096(A;A)
Reference Rs1057521096(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MITF
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.70014048G>A
CLNSRC
CLNACC RCV000442415.1,