SNP Report

Basic Info

Name	rs10242688 dbSNP Ensembl
Location	chr7:158943421 - 158943421(1)
Variant Alleles	C/G
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.119808
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000407559, ENST00000444851, ENST00000454771, ENST00000467220); NMD_transcript_variant(ENST00000444851, ENST00000454771); non_coding_transcript_variant(ENST00000467220)
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)
WDR60	WD repeat domain 60	7q36.3	1(0/1/0)

SNPs in LD with rs10242688 (count: 0) View in gBrowse (chr7:158943421..158943421 )

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

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