rs60687604
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | |
(G;G) | 0 | common in complete genomics |
Make rs60687604(A;A) |
Make rs60687604(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 52306237 |
Gene | KRT86 |
is a | snp |
is | mentioned by |
dbSNP | rs60687604 |
dbSNP (classic) | rs60687604 |
ClinGen | rs60687604 |
ebi | rs60687604 |
HLI | rs60687604 |
Exac | rs60687604 |
Gnomad | rs60687604 |
Varsome | rs60687604 |
LitVar | rs60687604 |
Map | rs60687604 |
PheGenI | rs60687604 |
Biobank | rs60687604 |
1000 genomes | rs60687604 |
hgdp | rs60687604 |
ensembl | rs60687604 |
geneview | rs60687604 |
scholar | rs60687604 |
rs60687604 | |
pharmgkb | rs60687604 |
gwascentral | rs60687604 |
openSNP | rs60687604 |
23andMe | rs60687604 |
SNPshot | rs60687604 |
SNPdbe | rs60687604 |
MSV3d | rs60687604 |
GWAS Ctlg | rs60687604 |
Merged from | Rs28939669 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs60687604(A;A) Rs60687604(C;C) |
Alt | rs60687604(A;A) Rs60687604(C;C) |
Reference | Rs60687604(G;G) |
Significance | Pathogenic |
Disease | Beaded hair not provided |
Variation | info |
Gene | KRT86 |
CLNDBN | Beaded hair not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.52700021G>A; NC_000012.11:g.52700021G>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000008050.3, RCV000056957.1, RCV000008052.3, RCV000056958.1, |