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rs1057517173

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517173(G;T)
Make rs1057517173(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position21577499
GeneALPL
is asnp
is mentioned by
dbSNPrs1057517173
dbSNP (old)rs1057517173
ClinGenrs1057517173
ebirs1057517173
HLIrs1057517173
Exacrs1057517173
Gnomadrs1057517173
Varsomers1057517173
Maprs1057517173
PheGenIrs1057517173
Biobankrs1057517173
1000 genomesrs1057517173
hgdprs1057517173
ensemblrs1057517173
gopubmedrs1057517173
geneviewrs1057517173
scholarrs1057517173
googlers1057517173
pharmgkbrs1057517173
gwascentralrs1057517173
openSNPrs1057517173
23andMers1057517173
23andMe allrs1057517173
SNPshotrs1057517173
SNPdbers1057517173
MSV3drs1057517173
GWAS Ctlgrs1057517173
Max Magnitude0
ClinVar
Risk rs1057517173(T;T)
Alt rs1057517173(T;T)
Reference Rs1057517173(G;G)
Significance Probable-Pathogenic
Disease Infantile hypophosphatasia
Variation info
Gene ALPL
CLNDBN Infantile hypophosphatasia
Reversed 0
HGVS NC_000001.10:g.21903992G>T
CLNSRC
CLNACC RCV000410612.1,