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SNP Report
Name | rs3823624 dbSNP Ensembl | ||
---|---|---|---|
Location | chr7:2070711 - 2070711(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.170128 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000265854, ENST00000399654, ENST00000402746, ENST00000406869, ENST00000421113, ENST00000438959, ENST00000444373, ENST00000464742, ENST00000483165, ENST00000491858); non_coding_transcript_variant(ENST00000464742, ENST00000483165, ENST00000491858) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |