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SNP Report
Name | rs10791345 dbSNP Ensembl | ||
---|---|---|---|
Location | chr11:134142118 - 134142118(1) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.154153 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000299106, ENST00000441717, ENST00000524969, ENST00000531302, ENST00000532165, ENST00000532252, ENST00000534549); NMD_transcript_variant(ENST00000532252); non_coding_transcript_variant(ENST00000524969, ENST00000531302, ENST00000532165) | ||
No. of Studies | 2 (Positive: 0; Negative: 1; Trend: 1) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.