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rs104894019

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894019(A;A)
Make rs104894019(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position27198258
GeneHOXA13
is asnp
is mentioned by
dbSNPrs104894019
ebirs104894019
HLIrs104894019
Exacrs104894019
Varsomers104894019
Maprs104894019
PheGenIrs104894019
hapmaprs104894019
1000 genomesrs104894019
hgdprs104894019
ensemblrs104894019
gopubmedrs104894019
geneviewrs104894019
scholarrs104894019
googlers104894019
pharmgkbrs104894019
gwascentralrs104894019
openSNPrs104894019
23andMers104894019
23andMe allrs104894019
SNP Nexus

SNPshotrs104894019
SNPdbers104894019
MSV3drs104894019
GWAS Ctlgrs104894019
Max Magnitude0
OMIM142959
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894019(A;A)
Alt rs104894019(A;A)
Reference rs104894019(G;G)
Significance Pathogenic
Disease Hand foot uterus syndrome
Variation info
Gene HOXA13
CLNDBN Hand foot uterus syndrome
Reversed 1
HGVS NC_000007.13:g.27237877C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000016018.25,