SNP Report

Basic Info

Name	rs2071436 dbSNP Ensembl
Location	chr22:23199301 - 23199301(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.226438
Functional Annotation	intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000305877, ENST00000359540, ENST00000398512, ENST00000463770, ENST00000479188); non_coding_transcript_exon_variant(ENST00000487679); non_coding_transcript_variant(ENST00000463770, ENST00000479188, ENST00000487679)
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)
BCR	breakpoint cluster region	22q11	2(1/1/0)

SNPs in LD with rs2071436 (count: 0) View in gBrowse (chr22:23199301..23199301 )

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

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