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rs1057518056

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518056(A;A)
Make rs1057518056(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position155803261
GeneSHH
is asnp
is mentioned by
dbSNPrs1057518056
dbSNP (old)rs1057518056
ClinGenrs1057518056
ebirs1057518056
HLIrs1057518056
Exacrs1057518056
Gnomadrs1057518056
Varsomers1057518056
LitVarrs1057518056
Maprs1057518056
PheGenIrs1057518056
Biobankrs1057518056
1000 genomesrs1057518056
hgdprs1057518056
ensemblrs1057518056
gopubmedrs1057518056
geneviewrs1057518056
scholarrs1057518056
googlers1057518056
pharmgkbrs1057518056
gwascentralrs1057518056
openSNPrs1057518056
23andMers1057518056
23andMe allrs1057518056
SNPshotrs1057518056
SNPdbers1057518056
MSV3drs1057518056
GWAS Ctlgrs1057518056
Max Magnitude0
ClinVar
Risk rs1057518056(A;A)
Alt rs1057518056(A;A)
Reference Rs1057518056(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SHH
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.155595955C>T
CLNSRC
CLNACC RCV000414014.1,