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rs137853021

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853021(G;T)
Make rs137853021(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position44942443
GeneSIX3
is asnp
is mentioned by
dbSNPrs137853021
ebirs137853021
HLIrs137853021
Exacrs137853021
Varsomers137853021
Maprs137853021
PheGenIrs137853021
hapmaprs137853021
1000 genomesrs137853021
hgdprs137853021
ensemblrs137853021
gopubmedrs137853021
geneviewrs137853021
scholarrs137853021
googlers137853021
pharmgkbrs137853021
gwascentralrs137853021
openSNPrs137853021
23andMers137853021
23andMe allrs137853021
SNP Nexus

SNPshotrs137853021
SNPdbers137853021
MSV3drs137853021
GWAS Ctlgrs137853021
Max Magnitude0
OMIM603714
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137853021(T;T)
Alt rs137853021(T;T)
Reference rs137853021(G;G)
Significance Pathogenic
Disease Holoprosencephaly 2
Variation info
Gene SIX3 SIX3-AS1
CLNDBN Holoprosencephaly 2
Reversed 0
HGVS NC_000002.11:g.45169582G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006472.2,