SNP Report

Basic Info
Name |
rs10232372
dbSNP
Ensembl
|
Location |
7:30587902 - 30587902(+) |
Variant Seq |
T |
Ancestral Allele |
G |
Ref Seq |
G |
Minor Allele Frequence |
0.404752 |
Annotation |
upstream_gene_variant; intron_variant; non_coding_transcript_variant
|
Variant Effect |
upstream_gene_variant(ENST00000454922); intron_variant(ENST00000584372, ENST00000582549, ENST00000582733, ENST00000579174, ENST00000578994, ENST00000580440, ENST00000426529, ENST00000584199, ENST00000581794, ENST00000581665, ENST00000583664); non_coding_transcript_variant(ENST00000584372, ENST00000582549, ENST00000582733, ENST00000579174, ENST00000578994, ENST00000580440, ENST00000426529, ENST00000584199, ENST00000581794, ENST00000581665, ENST00000583664)
|
SIFT Annotation |
tolerated
|
SIFT Variant Effect |
tolerated(LRG_243t1, ENST00000389266)
|
PolyPhen Annotation |
unknown
|
PolyPhen Variant Effect |
unknown(ENST00000627489, ENST00000454308)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
Chromatin interactive region
|
Chromatin State |
Weak transcription;Strong transcription;ZNF genes & repeats
|
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 rs10232372 (count: 0)

SNP related eQTL (count: 1)