rs786200937
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(GTAAATTT;GTAAATTT) | 0 | common in clinvar |
(I;I) | 0 | common genotype |
(TAAATTTG;TAAATTTG) | 0 | common in clinvar |
Make rs786200937(-;-) |
Make rs786200937(-;TAAATTTG) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 109741499 |
Gene | FIG4 |
is a | snp |
is | mentioned by |
dbSNP | rs786200937 |
dbSNP (classic) | rs786200937 |
ClinGen | rs786200937 |
ebi | rs786200937 |
HLI | rs786200937 |
Exac | rs786200937 |
Gnomad | rs786200937 |
Varsome | rs786200937 |
LitVar | rs786200937 |
Map | rs786200937 |
PheGenI | rs786200937 |
Biobank | rs786200937 |
1000 genomes | rs786200937 |
hgdp | rs786200937 |
ensembl | rs786200937 |
geneview | rs786200937 |
scholar | rs786200937 |
rs786200937 | |
pharmgkb | rs786200937 |
gwascentral | rs786200937 |
openSNP | rs786200937 |
23andMe | rs786200937 |
SNPshot | rs786200937 |
SNPdbe | rs786200937 |
MSV3d | rs786200937 |
GWAS Ctlg | rs786200937 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786200937(-;-) Rs786200937(GTAAATTT;GTAAATTT) |
Alt | rs786200937(-;-) Rs786200937(GTAAATTT;GTAAATTT) |
Reference | Rs786200937(TAAATTTG;TAAATTTG) |
Significance | Pathogenic |
Disease | Yunis Varon syndrome not provided |
Variation | info |
Gene | FIG4 |
CLNDBN | Yunis Varon syndrome not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.110062702_110062709delTAAATTTG |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000043691.4, RCV000236453.2, |