SNP Report

Basic Info

Name	rs1295111 dbSNP Ensembl
Location	chr1:5986372 - 5986372(1)
Variant Alleles	C/G
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.38778
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000378156, ENST00000378169, ENST00000478423, ENST00000489180, ENST00000622020); NMD_transcript_variant(ENST00000378169, ENST00000489180); non_coding_transcript_variant(ENST00000478423)
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)
NPHP4	nephronophthisis 4	1p36	1(1/0/0)

SNPs in LD with rs1295111 (count: 0) View in gBrowse (chr1:5986372..5986372 )

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

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