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Human (GRCh38.p14)
Most severe consequence
 
3 prime UTR variant
Alleles
CCCCCCC/CCCCCC/CCCCCCCC/CCCCCCCCC/CCCCCCCCTGCCCCCC... Click the plus to show all of the alleles|Ancestral: CCCCCCC|Highest population MAF: 0.49
Change tolerance
GERP: 0.10
Location

Chromosome 22:19968740-19968746 (forward strand)|VCF:22  19968740  rs397758621  CC  C,CCC,CCCC,CCCCCCCCTGCCC

Evidence status

Clinical significance

HGVS names

This variant has 12 HGVS names - Show

Synonyms

This variant has 10 synonyms - Show

Original source

Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP

About this variant

This variant has predicted consequences for 2 transcripts, has 3009 sample genotypes, is associated with 2 phenotypes and is mentioned in 9 citations.