SNP Report

Basic Info

Name	rs1979572 dbSNP Ensembl
Location	chr17:30184960 - 30184960(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.41873
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; synonymous_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000394826, ENST00000475652); downstream_gene_variant(ENST00000577289, ENST00000580103); NMD_transcript_variant(ENST00000394826, ENST00000475652); non_coding_transcript_exon_variant(ENST00000540900); non_coding_transcript_variant(ENST00000540900); synonymous_variant(ENST00000247026, ENST00000612959)
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 rs1979572 (count: 0) View in gBrowse (chr17:30184960..30184960 )

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

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