SNP Report

Basic Info

Name	rs9902340 dbSNP Ensembl
Location	chr17:30149440 - 30149440(1)
Variant Alleles	T/G
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.364018
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	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); upstream_gene_variant(ENST00000591928)
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 rs9902340 (count: 0) View in gBrowse (chr17:30149440..30149440 )

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

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