Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057517966

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517966(C;T)
Make rs1057517966(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position69959325
GeneMITF
is asnp
is mentioned by
dbSNPrs1057517966
dbSNP (old)rs1057517966
ClinGenrs1057517966
ebirs1057517966
HLIrs1057517966
Exacrs1057517966
Gnomadrs1057517966
Varsomers1057517966
LitVarrs1057517966
Maprs1057517966
PheGenIrs1057517966
Biobankrs1057517966
1000 genomesrs1057517966
hgdprs1057517966
ensemblrs1057517966
gopubmedrs1057517966
geneviewrs1057517966
scholarrs1057517966
googlers1057517966
pharmgkbrs1057517966
gwascentralrs1057517966
openSNPrs1057517966
23andMers1057517966
23andMe allrs1057517966
SNPshotrs1057517966
SNPdbers1057517966
MSV3drs1057517966
GWAS Ctlgrs1057517966
Max Magnitude0
ClinVar
Risk rs1057517966(T;T)
Alt rs1057517966(T;T)
Reference Rs1057517966(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MITF
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.70008476C>T
CLNSRC
CLNACC RCV000413197.1,