SNP Report

Basic Info
Name |
rs740601
dbSNP
Ensembl
|
Location |
22:19963240 - 19963240(+) |
Variant Seq |
G |
Ancestral Allele |
G |
Ref Seq |
T |
Minor Allele Frequence |
0.36861 |
Annotation |
downstream_gene_variant; upstream_gene_variant; intron_variant; NMD_transcript_variant
|
Variant Effect |
downstream_gene_variant(ENST00000467943); upstream_gene_variant(ENST00000585066, ENST00000493893, ENST00000428707); intron_variant(ENST00000407537, ENST00000449653, ENST00000403184, ENST00000406520, ENST00000207636, ENST00000412786, ENST00000403710, ENST00000361682); NMD_transcript_variant(ENST00000207636)
|
SIFT Annotation |
deleterious
|
SIFT Variant Effect |
deleterious(ENST00000412786, ENST00000403184, ENST00000449653, ENST00000406520, ENST00000361682, ENST00000207636, ENST00000407537, ENST00000403710)
|
PolyPhen Annotation |
possibly_damaging; probably_damaging
|
PolyPhen Variant Effect |
possibly_damaging(ENST00000207636); probably_damaging(ENST00000412786, ENST00000403184, ENST00000449653, ENST00000406520, ENST00000361682, ENST00000407537, ENST00000403710)
|
rSNP? |
No
Link in rVarBase
|
Related Regulatory Elements |
N.A.
|
Chromatin State |
N.A.
|
No. of Marker's Association Results |
0 (Positive: 0; Negative: 0; Trend: 0) |
Source |
LD-proxy |

SNP related association results

SNP related genes (count: 1)

SNPs in LD with rs740601 (count: 0)

SNP related eQTL (count: 1)