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rs137853341

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853341(A;A)
Make rs137853341(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position155803142
GeneSHH
is asnp
is mentioned by
dbSNPrs137853341
ebirs137853341
HLIrs137853341
Exacrs137853341
Varsomers137853341
Maprs137853341
PheGenIrs137853341
hapmaprs137853341
1000 genomesrs137853341
hgdprs137853341
ensemblrs137853341
gopubmedrs137853341
geneviewrs137853341
scholarrs137853341
googlers137853341
pharmgkbrs137853341
gwascentralrs137853341
openSNPrs137853341
23andMers137853341
23andMe allrs137853341
SNP Nexus

SNPshotrs137853341
SNPdbers137853341
MSV3drs137853341
GWAS Ctlgrs137853341
Max Magnitude0
OMIM600725
Desc
Variant0010
Relatedalso
ClinVar
Risk rs137853341(A;A)
Alt rs137853341(A;A)
Reference rs137853341(G;G)
Significance Pathogenic
Disease Holoprosencephaly 3
Variation info
Gene SHH
CLNDBN Holoprosencephaly 3
Reversed 1
HGVS NC_000007.13:g.155595836C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009436.2,