rs104893956
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 3 | Carrier for an estrogen resistance mutation |
Make rs104893956(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 151842613 |
Gene | ESR1 |
is a | snp |
is | mentioned by |
dbSNP | rs104893956 |
dbSNP (classic) | rs104893956 |
ClinGen | rs104893956 |
ebi | rs104893956 |
HLI | rs104893956 |
Exac | rs104893956 |
Gnomad | rs104893956 |
Varsome | rs104893956 |
LitVar | rs104893956 |
Map | rs104893956 |
PheGenI | rs104893956 |
Biobank | rs104893956 |
1000 genomes | rs104893956 |
hgdp | rs104893956 |
ensembl | rs104893956 |
geneview | rs104893956 |
scholar | rs104893956 |
rs104893956 | |
pharmgkb | rs104893956 |
gwascentral | rs104893956 |
openSNP | rs104893956 |
23andMe | rs104893956 |
SNPshot | rs104893956 |
SNPdbe | rs104893956 |
MSV3d | rs104893956 |
GWAS Ctlg | rs104893956 |
Max Magnitude | 3 |
see OMIM 133430.0002
ClinVar | |
---|---|
Risk | rs104893956(T;T) |
Alt | rs104893956(T;T) |
Reference | Rs104893956(C;C) |
Significance | Pathogenic |
Disease | Estrogen resistance |
Variation | info |
Gene | ESR1 |
CLNDBN | Estrogen resistance |
Reversed | 0 |
HGVS | NC_000006.11:g.152163748C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000018060.29, |