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rs118204055

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs118204055(C;C)
Make rs118204055(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position128330896
GeneRBM28
is asnp
is mentioned by
dbSNPrs118204055
ebirs118204055
HLIrs118204055
Exacrs118204055
Varsomers118204055
Maprs118204055
PheGenIrs118204055
hapmaprs118204055
1000 genomesrs118204055
hgdprs118204055
ensemblrs118204055
gopubmedrs118204055
geneviewrs118204055
scholarrs118204055
googlers118204055
pharmgkbrs118204055
gwascentralrs118204055
openSNPrs118204055
23andMers118204055
23andMe allrs118204055
SNP Nexus

SNPshotrs118204055
SNPdbers118204055
MSV3drs118204055
GWAS Ctlgrs118204055
Max Magnitude0
OMIM612074
Desc
Variant0001
Relatedalso
ClinVar
Risk rs118204055(C;C)
Alt rs118204055(C;C)
Reference rs118204055(T;T)
Significance Pathogenic
Disease Alopecia
Variation info
Gene RBM28
CLNDBN Alopecia, neurologic defects, and endocrinopathy syndrome
Reversed 1
HGVS NC_000007.13:g.127970949A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000768.4,