SNP Report

Basic Info

Name	rs16861997 dbSNP Ensembl
Location	chr1:169189742 - 169189742(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.176318
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000367811, ENST00000472647, ENST00000483228, ENST00000493481, ENST00000525440, ENST00000530739); NMD_transcript_variant(ENST00000525440); non_coding_transcript_variant(ENST00000483228, ENST00000493481, ENST00000530739)
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)
NME7	NME/NM23 family member 7	1q24.2	1(0/1/0)

SNPs in LD with rs16861997 (count: 0) View in gBrowse (chr1:169189742..169189742 )

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

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