SNP Report

Basic Info

Name	rs3135737 dbSNP Ensembl
Location	chr10:121553445 - 121553445(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.117612
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000336553, ENST00000346997, ENST00000351936, ENST00000356226, ENST00000357555, ENST00000358487, ENST00000359354, ENST00000360144, ENST00000369056, ENST00000369058, ENST00000369059, ENST00000369060, ENST00000369061, ENST00000457416, ENST00000490349, ENST00000604236, ENST00000613048); NMD_transcript_variant(ENST00000604236); non_coding_transcript_variant(ENST00000490349)
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)
FGFR2	fibroblast growth factor receptor 2	10q25.3-q26	2(1/1/0)

SNPs in LD with rs3135737 (count: 0) View in gBrowse (chr10:121553445..121553445 )

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

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