SNP Report

Basic Info

Name	rs587948 dbSNP Ensembl
Location	chr8:127329435 - 127329435(1)
Variant Alleles	T/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.480631
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000501396, ENST00000502082, ENST00000523825); non_coding_transcript_variant(ENST00000501396, ENST00000502082, ENST00000523825)
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)
CASC8	cancer susceptibility candidate 8 (non-protein coding)	8q24.21	Mapped by Literature SNP

SNPs in LD with rs587948 (count: 0) View in gBrowse (chr8:127329435..127329435 )

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

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