rs28935770
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs28935770(A;G) |
Make rs28935770(G;G) |
Reference | GRCh37 37.1/131 |
Chromosome | 6 |
Position | 54635555 |
Gene | KRAS1P |
is a | snp |
is | mentioned by |
dbSNP | rs28935770 |
dbSNP (classic) | rs28935770 |
ClinGen | rs28935770 |
ebi | rs28935770 |
HLI | rs28935770 |
Exac | rs28935770 |
Gnomad | rs28935770 |
Varsome | rs28935770 |
LitVar | rs28935770 |
Map | rs28935770 |
PheGenI | rs28935770 |
Biobank | rs28935770 |
1000 genomes | rs28935770 |
hgdp | rs28935770 |
ensembl | rs28935770 |
geneview | rs28935770 |
scholar | rs28935770 |
rs28935770 | |
pharmgkb | rs28935770 |
gwascentral | rs28935770 |
openSNP | rs28935770 |
23andMe | rs28935770 |
SNPshot | rs28935770 |
SNPdbe | rs28935770 |
MSV3d | rs28935770 |
GWAS Ctlg | rs28935770 |
Status | Deleted |
Max Magnitude | 0 |
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP