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Select item 38328501.

rs3832850 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTT>-,CTTCTT [Show Flanks]
Chromosome:: 12:9099232 (GRCh38)
12:9251828 (GRCh37)
Canonical SPDI:: NC_000012.12:9099228:CTTCTT:CTT,NC_000012.12:9099228:CTTCTT:CTTCTTCTT
Gene:: A2M (Varview), KLRG1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTTCTT=0.361609/6697 (ALFA)
-=0.067881/5257 (TOMMO)
-=0.075615/547 (Korea4K)
-=0.083333/18 (Vietnamese)
-=0.258786/1296 (1000Genomes)
-=0.267489/1713 (1000Genomes_30X)
-=0.330519/87485 (TOPMED)
-=0.334115/49727 (GnomAD_genomes)
-=0.340885/1264 (TWINSUK)
-=0.342685/342 (GoNL)
-=0.346653/1336 (ALSPAC)
-=0.35/14 (GENOME_DK)
-=0.366667/220 (NorthernSweden)
-=0.406696/1822 (Estonian)
HGVS:: NC_000012.12:g.9099229CTT[1], NC_000012.12:g.9099229CTT[3], NC_000012.11:g.9251825CTT[1], NC_000012.11:g.9251825CTT[3], NG_011717.2:g.21729AAG[1], NG_011717.2:g.21729AAG[3]

Supplemental Content

dbSNP