SNP Report

Basic Info

Name	rs127196 dbSNP Ensembl
Location	chr6:152406196 - 152406196(1)
Variant Alleles	C/A
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.4998
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000458194); intron_variant(ENST00000341594, ENST00000367255, ENST00000423061, ENST00000461872, ENST00000535081); non_coding_transcript_variant(ENST00000461872, ENST00000535081); upstream_gene_variant(ENST00000365174)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
SYNE1	spectrin repeat containing, nuclear envelope 1	6q25.2	6(3/2/1)
RNA5SP223	RNA, 5S ribosomal pseudogene 223	6q25.2	Mapped by LD-proxy

SNPs in LD with rs127196 (count: 0) View in gBrowse (chr6:152406196..152406196 )

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

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