rs151339002
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs151339002(G;T) |
Make rs151339002(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 103329863 |
Gene | FZD6 |
is a | snp |
is | mentioned by |
dbSNP | rs151339002 |
dbSNP (classic) | rs151339002 |
ClinGen | rs151339002 |
ebi | rs151339002 |
HLI | rs151339002 |
Exac | rs151339002 |
Gnomad | rs151339002 |
Varsome | rs151339002 |
LitVar | rs151339002 |
Map | rs151339002 |
PheGenI | rs151339002 |
Biobank | rs151339002 |
1000 genomes | rs151339002 |
hgdp | rs151339002 |
ensembl | rs151339002 |
geneview | rs151339002 |
scholar | rs151339002 |
rs151339002 | |
pharmgkb | rs151339002 |
gwascentral | rs151339002 |
openSNP | rs151339002 |
23andMe | rs151339002 |
SNPshot | rs151339002 |
SNPdbe | rs151339002 |
MSV3d | rs151339002 |
GWAS Ctlg | rs151339002 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs151339002(A;A) rs151339002(T;T) |
Alt | rs151339002(A;A) rs151339002(T;T) |
Reference | Rs151339002(G;G) |
Significance | Pathogenic |
Disease | Nail disorder Nail disease |
Variation | info |
Gene | FZD6 |
CLNDBN | Nail disorder, nonsyndromic congenital, 10 Nail disease |
Reversed | 0 |
HGVS | NC_000008.10:g.104342091G>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000023300.2, RCV000077802.1, |