rs142703147
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs142703147(A;A) |
Make rs142703147(A;C) |
Make rs142703147(C;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 147835718 |
Gene | SPINK1 |
is a | snp |
is | mentioned by |
dbSNP | rs142703147 |
dbSNP (classic) | rs142703147 |
ClinGen | rs142703147 |
ebi | rs142703147 |
HLI | rs142703147 |
Exac | rs142703147 |
Gnomad | rs142703147 |
Varsome | rs142703147 |
LitVar | rs142703147 |
Map | rs142703147 |
PheGenI | rs142703147 |
Biobank | rs142703147 |
1000 genomes | rs142703147 |
hgdp | rs142703147 |
ensembl | rs142703147 |
geneview | rs142703147 |
scholar | rs142703147 |
rs142703147 | |
pharmgkb | rs142703147 |
gwascentral | rs142703147 |
openSNP | rs142703147 |
23andMe | rs142703147 |
SNPshot | rs142703147 |
SNPdbe | rs142703147 |
MSV3d | rs142703147 |
GWAS Ctlg | rs142703147 |
Max Magnitude | 0 |
[PMID 28556356] Identification of a functional enhancer variant within the chronic pancreatitis-associated SPINK1 c.101A>G (p.Asn34Ser)-containing haplotype.