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SNP Report
Name | rs6975291 dbSNP Ensembl | ||
---|---|---|---|
Location | chr7:148851301 - 148851301(1) | ||
Variant Alleles | C/G | ||
Ancestral Allele | G | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.229233 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000320356, ENST00000350995, ENST00000460911, ENST00000476773, ENST00000478654, ENST00000483012, ENST00000483967, ENST00000492143, ENST00000498186, LRG_531t1); NMD_transcript_variant(ENST00000483012, ENST00000492143); non_coding_transcript_variant(ENST00000498186) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |