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SNP Report
Name | rs993639 dbSNP Ensembl | ||
---|---|---|---|
Location | chr8:101956088 - 101956088(1) | ||
Variant Alleles | A/G | ||
Ancestral Allele | G | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.320887 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000311028, ENST00000395923, ENST00000517531, ENST00000517639, ENST00000517822, ENST00000518166, ENST00000518661, ENST00000518727, ENST00000518952, ENST00000520425, ENST00000520690, ENST00000521599, ENST00000521964, ENST00000522078, ENST00000522206, ENST00000523923, ENST00000524209); non_coding_transcript_variant(ENST00000517639, ENST00000518952) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |