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SNP Report
Name | rs10269829 dbSNP Ensembl | ||
---|---|---|---|
Location | chr7:64218984 - 64218984(1) | ||
Variant Alleles | A/G | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.0605032 | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000429565) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |