BDgene

SNP Report

Basic Info
Name rs9896012 dbSNP Ensembl
Location chr17:30143073 - 30143073(1)
Variant Alleles T/C
Ancestral Allele C
Minor Allele T
Minor Allele Frequence 0.364417
Functional Annotation downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000591928); intron_variant(ENST00000247026, ENST00000394826, ENST00000467446, ENST00000475652, ENST00000540900, ENST00000577289, ENST00000580103, ENST00000581048, ENST00000583301, ENST00000584154, ENST00000584317, ENST00000585881, ENST00000588614, ENST00000589608, ENST00000612959); NMD_transcript_variant(ENST00000394826, ENST00000475652, ENST00000584154, ENST00000584317, ENST00000589608); non_coding_transcript_variant(ENST00000467446, ENST00000540900, ENST00000577289, ENST00000581048, ENST00000583301)
No. of Studies 0 (Positive: 0; Negative: 0; Trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
NSRP1 nuclear speckle splicing regulatory protein 1 17q11.2 Mapped by Literature SNP

SNPs in LD with rs9896012 (count: 0) View in gBrowse (chr17:30143073..30143073 )

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)