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rs137853099

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853099(A;A)
Make rs137853099(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position151344444
GeneRFX5
is asnp
is mentioned by
dbSNPrs137853099
ebirs137853099
HLIrs137853099
Exacrs137853099
Varsomers137853099
Maprs137853099
PheGenIrs137853099
hapmaprs137853099
1000 genomesrs137853099
hgdprs137853099
ensemblrs137853099
gopubmedrs137853099
geneviewrs137853099
scholarrs137853099
googlers137853099
pharmgkbrs137853099
gwascentralrs137853099
openSNPrs137853099
23andMers137853099
23andMe allrs137853099
SNP Nexus

SNPshotrs137853099
SNPdbers137853099
MSV3drs137853099
GWAS Ctlgrs137853099
Max Magnitude0
OMIM601863
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137853099(A;A)
Alt rs137853099(A;A)
Reference rs137853099(G;G)
Significance Pathogenic
Disease Bare lymphocyte syndrome type 2
Variation info
Gene RFX5
CLNDBN Bare lymphocyte syndrome type 2, complementation group E
Reversed 1
HGVS NC_000001.10:g.151316920C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008087.2,