SNP Report

Basic Info

Name	rs7342921 dbSNP Ensembl
Location	chr17:30285430 - 30285430(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.26877
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(ENST00000578090); downstream_gene_variant(ENST00000410747, ENST00000577290, ENST00000580709); NMD_transcript_variant(ENST00000578090); non_coding_transcript_exon_variant(ENST00000579325, ENST00000582669); non_coding_transcript_variant(ENST00000579325, ENST00000582669); synonymous_variant(ENST00000261714, ENST00000577623, ENST00000581037, ENST00000584603)
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)
BLMH	bleomycin hydrolase	17q11.2	Mapped by Literature SNP
RNU6-1267P	RNA, U6 small nuclear 1267, pseudogene	17q11.2	Mapped by Literature SNP

SNPs in LD with rs7342921 (count: 0) View in gBrowse (chr17:30285430..30285430 )

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

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