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rs17147033

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17147033(C;T)
Make rs17147033(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position124366686
is asnp
is mentioned by
dbSNPrs17147033
ebirs17147033
HLIrs17147033
Exacrs17147033
Varsomers17147033
Maprs17147033
PheGenIrs17147033
hapmaprs17147033
1000 genomesrs17147033
hgdprs17147033
ensemblrs17147033
gopubmedrs17147033
geneviewrs17147033
scholarrs17147033
googlers17147033
pharmgkbrs17147033
gwascentralrs17147033
openSNPrs17147033
23andMers17147033
23andMe allrs17147033
SNP Nexus

SNPshotrs17147033
SNPdbers17147033
MSV3drs17147033
GWAS Ctlgrs17147033
GMAF0.1079
Max Magnitude0
? (C;C) (C;T) (T;T) 28
OMIM612079
DescALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME
Variant
Relatedalso