Name: rs68166392
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs68166392

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:106187508-106187511 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: delTT / dupT / dupTT / insTTC(T)₅ …
delTT / dupT / dupTT / insTTC(T)₅ / insTTC(T)₆ / insTTC(T)₈ / dupTTT / dup(T)₄ / ins(T)₇ / ins(T)₈ / ins(T)₉
Variation Type: Indel Insertion and Deletion
Frequency: (T)₄=0.2985 (1760/5896, ALFA)
(T)₄=0.0290 (145/5008, 1000G)
(T)₄=0.044 (26/592, NorthernSweden) (+ 1 more)
(T)₄=0.12 (5/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC02624 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	5896	TTTT=0.2985	TT=0.0003, TTTTT=0.0000, TTTTTT=0.7012, TTTTTTCTTTTTT=0.0000	0.27427	0.67685	0.04888	32
European	Sub	4508	TTTT=0.0843	TT=0.0004, TTTTT=0.0000, TTTTTT=0.9153, TTTTTTCTTTTTT=0.0000	0.052398	0.883659	0.063943	32
African	Sub	1290	TTTT=1.0000	TT=0.0000, TTTTT=0.0000, TTTTTT=0.0000, TTTTTTCTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	66	TTTT=1.00	TT=0.00, TTTTT=0.00, TTTTTT=0.00, TTTTTTCTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1224	TTTT=1.0000	TT=0.0000, TTTTT=0.0000, TTTTTT=0.0000, TTTTTTCTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	6	TTTT=1.0	TT=0.0, TTTTT=0.0, TTTTTT=0.0, TTTTTTCTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	6	TTTT=1.0	TT=0.0, TTTTT=0.0, TTTTTT=0.0, TTTTTTCTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTT=0	TT=0, TTTTT=0, TTTTTT=0, TTTTTTCTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	10	TTTT=1.0	TT=0.0, TTTTT=0.0, TTTTTT=0.0, TTTTTTCTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	30	TTTT=1.00	TT=0.00, TTTTT=0.00, TTTTTT=0.00, TTTTTTCTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	0	TTTT=0	TT=0, TTTTT=0, TTTTTT=0, TTTTTTCTTTTTT=0	0	0	0	N/A
Other	Sub	52	TTTT=0.85	TT=0.00, TTTTT=0.00, TTTTTT=0.15, TTTTTTCTTTTTT=0.00	0.846154	0.153846	0.0	14

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	5896	(T)₄=0.2985	delTT=0.0003, dupT=0.0000, dupTT=0.7012, insTTC(T)₆=0.0000
Allele Frequency Aggregator	European	Sub	4508	(T)₄=0.0843	delTT=0.0004, dupT=0.0000, dupTT=0.9153, insTTC(T)₆=0.0000
Allele Frequency Aggregator	African	Sub	1290	(T)₄=1.0000	delTT=0.0000, dupT=0.0000, dupTT=0.0000, insTTC(T)₆=0.0000
Allele Frequency Aggregator	Other	Sub	52	(T)₄=0.85	delTT=0.00, dupT=0.00, dupTT=0.15, insTTC(T)₆=0.00
Allele Frequency Aggregator	Latin American 2	Sub	30	(T)₄=1.00	delTT=0.00, dupT=0.00, dupTT=0.00, insTTC(T)₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	10	(T)₄=1.0	delTT=0.0, dupT=0.0, dupTT=0.0, insTTC(T)₆=0.0
Allele Frequency Aggregator	Asian	Sub	6	(T)₄=1.0	delTT=0.0, dupT=0.0, dupTT=0.0, insTTC(T)₆=0.0
Allele Frequency Aggregator	South Asian	Sub	0	(T)₄=0	delTT=0, dupT=0, dupTT=0, insTTC(T)₆=0
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupTT=0.9710
1000Genomes	African	Sub	1322	- No frequency provided	dupTT=0.9796
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupTT=0.8968
1000Genomes	Europe	Sub	1006	- No frequency provided	dupTT=1.0000
1000Genomes	South Asian	Sub	978	- No frequency provided	dupTT=0.997
1000Genomes	American	Sub	694	- No frequency provided	dupTT=0.984
Northern Sweden	ACPOP	Study-wide	592	- No frequency provided	dupTT=0.956
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupTT=0.88

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 10	NC_000010.11:g.106187510_106187511del
GRCh38.p14 chr 10	NC_000010.11:g.106187511dup
GRCh38.p14 chr 10	NC_000010.11:g.106187510_106187511dup
GRCh38.p14 chr 10	NC_000010.11:g.106187508_106187511T[6]CTTTTT[1]
GRCh38.p14 chr 10	NC_000010.11:g.106187508_106187511T[6]CTTTTTT[1]
GRCh38.p14 chr 10	NC_000010.11:g.106187508_106187511T[6]CTTTTTTTT[1]
GRCh38.p14 chr 10	NC_000010.11:g.106187509_106187511dup
GRCh38.p14 chr 10	NC_000010.11:g.106187508_106187511dup
GRCh38.p14 chr 10	NC_000010.11:g.106187511_106187512insTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.106187511_106187512insTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.106187511_106187512insTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.107947268_107947269del
GRCh37.p13 chr 10	NC_000010.10:g.107947269dup
GRCh37.p13 chr 10	NC_000010.10:g.107947268_107947269dup
GRCh37.p13 chr 10	NC_000010.10:g.107947266_107947269T[6]CTTTTT[1]
GRCh37.p13 chr 10	NC_000010.10:g.107947266_107947269T[6]CTTTTTT[1]
GRCh37.p13 chr 10	NC_000010.10:g.107947266_107947269T[6]CTTTTTTTT[1]
GRCh37.p13 chr 10	NC_000010.10:g.107947267_107947269dup
GRCh37.p13 chr 10	NC_000010.10:g.107947266_107947269dup
GRCh37.p13 chr 10	NC_000010.10:g.107947269_107947270insTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.107947269_107947270insTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.107947269_107947270insTTTTTTTTT

Gene: LINC02624, long intergenic non-protein coding RNA 2624 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC02624 transcript variant 2	NR_134330.1:n.	N/A	Intron Variant
LINC02624 transcript variant 1	NR_134329.1:n.	N/A	Genic Downstream Transcript Variant
LINC02624 transcript variant 3	NR_134331.1:n.	N/A	Genic Downstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₄=	delTT	dupT	dupTT	insTTC(T)₅	insTTC(T)₆	insTTC(T)₈	dupTTT	dup(T)₄	ins(T)₇	ins(T)₈	ins(T)₉
GRCh38.p14 chr 10	NC_000010.11:g.106187508_106187511=	NC_000010.11:g.106187510_106187511del	NC_000010.11:g.106187511dup	NC_000010.11:g.106187510_106187511dup	NC_000010.11:g.106187508_106187511T[6]CTTTTT[1]	NC_000010.11:g.106187508_106187511T[6]CTTTTTT[1]	NC_000010.11:g.106187508_106187511T[6]CTTTTTTTT[1]	NC_000010.11:g.106187509_106187511dup	NC_000010.11:g.106187508_106187511dup	NC_000010.11:g.106187511_106187512insTTTTTTT	NC_000010.11:g.106187511_106187512insTTTTTTTT	NC_000010.11:g.106187511_106187512insTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.107947266_107947269=	NC_000010.10:g.107947268_107947269del	NC_000010.10:g.107947269dup	NC_000010.10:g.107947268_107947269dup	NC_000010.10:g.107947266_107947269T[6]CTTTTT[1]	NC_000010.10:g.107947266_107947269T[6]CTTTTTT[1]	NC_000010.10:g.107947266_107947269T[6]CTTTTTTTT[1]	NC_000010.10:g.107947267_107947269dup	NC_000010.10:g.107947266_107947269dup	NC_000010.10:g.107947269_107947270insTTTTTTT	NC_000010.10:g.107947269_107947270insTTTTTTTT	NC_000010.10:g.107947269_107947270insTTTTTTTTT

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

63 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80839272	Oct 12, 2018 (152)
2	HUMANGENOME_JCVI	ss95551993	Oct 12, 2018 (152)
3	BL	ss256137088	May 09, 2011 (138)
4	GMI	ss287865291	Oct 12, 2018 (152)
5	GMI	ss289035787	Oct 12, 2018 (152)
6	PJP	ss294674925	May 09, 2011 (137)
7	1000GENOMES	ss327276797	May 09, 2011 (138)
8	1000GENOMES	ss327359826	May 09, 2011 (138)
9	LUNTER	ss552065179	Apr 25, 2013 (138)
10	LUNTER	ss553426283	Apr 25, 2013 (138)
11	SSMP	ss663949760	Apr 01, 2015 (144)
12	BILGI_BIOE	ss666514822	Apr 25, 2013 (138)
13	1000GENOMES	ss1370063358	Aug 21, 2014 (142)
14	DDI	ss1536667760	Apr 01, 2015 (144)
15	EVA_GENOME_DK	ss1574256501	Apr 01, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1706887089	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1706887091	Apr 01, 2015 (144)
18	EVA_UK10K_ALSPAC	ss1706887092	Apr 01, 2015 (144)
19	EVA_UK10K_TWINSUK	ss1706887241	Apr 01, 2015 (144)
20	EVA_UK10K_TWINSUK	ss1706887244	Apr 01, 2015 (144)
21	EVA_UK10K_TWINSUK	ss1706887247	Apr 01, 2015 (144)
22	JJLAB	ss2031041590	Sep 14, 2016 (149)
23	SYSTEMSBIOZJU	ss2627644719	Nov 08, 2017 (151)
24	SWEGEN	ss3007093543	Jan 10, 2018 (151)
25	MCHAISSO	ss3063668226	Nov 08, 2017 (151)
26	MCHAISSO	ss3064490360	Nov 08, 2017 (151)
27	MCHAISSO	ss3065401538	Nov 08, 2017 (151)
28	BEROUKHIMLAB	ss3644306892	Oct 12, 2018 (152)
29	BIOINF_KMB_FNS_UNIBA	ss3645160817	Oct 12, 2018 (152)
30	EVA_DECODE	ss3690616729	Jul 13, 2019 (153)
31	EVA_DECODE	ss3690616730	Jul 13, 2019 (153)
32	EVA_DECODE	ss3690616731	Jul 13, 2019 (153)
33	EVA_DECODE	ss3690616736	Jul 13, 2019 (153)
34	EVA_DECODE	ss3690616737	Jul 13, 2019 (153)
35	EVA_DECODE	ss3690616742	Jul 13, 2019 (153)
36	EVA_DECODE	ss3690616743	Jul 13, 2019 (153)
37	ACPOP	ss3737650622	Jul 13, 2019 (153)
38	PACBIO	ss3786778313	Jul 13, 2019 (153)
39	PACBIO	ss3791941818	Jul 13, 2019 (153)
40	PACBIO	ss3796823913	Jul 13, 2019 (153)
41	KHV_HUMAN_GENOMES	ss3813921375	Jul 13, 2019 (153)
42	EVA	ss3832315061	Apr 26, 2020 (154)
43	GNOMAD	ss4225019965	Apr 26, 2021 (155)
44	GNOMAD	ss4225019966	Apr 26, 2021 (155)
45	GNOMAD	ss4225019967	Apr 26, 2021 (155)
46	GNOMAD	ss4225019968	Apr 26, 2021 (155)
47	GNOMAD	ss4225019970	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5199327899	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5199327900	Apr 26, 2021 (155)
50	1000G_HIGH_COVERAGE	ss5285350641	Oct 13, 2022 (156)
51	HUGCELL_USP	ss5480785725	Oct 13, 2022 (156)
52	SANFORD_IMAGENETICS	ss5650029573	Oct 13, 2022 (156)
53	TOMMO_GENOMICS	ss5745655712	Oct 13, 2022 (156)
54	TOMMO_GENOMICS	ss5745655713	Oct 13, 2022 (156)
55	TOMMO_GENOMICS	ss5745655714	Oct 13, 2022 (156)
56	YY_MCH	ss5811856132	Oct 13, 2022 (156)
57	EVA	ss5824913048	Oct 13, 2022 (156)
58	EVA	ss5824913049	Oct 13, 2022 (156)
59	EVA	ss5824913050	Oct 13, 2022 (156)
60	EVA	ss5824913052	Oct 13, 2022 (156)
61	EVA	ss5849726512	Oct 13, 2022 (156)
62	EVA	ss5880389695	Oct 13, 2022 (156)
63	EVA	ss5980637086	Oct 13, 2022 (156)
64	1000Genomes	NC_000010.10 - 107947266	Oct 12, 2018 (152)
65	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 28526894 (NC_000010.10:107947265::TTTTTTT 157/3854) Row 28526895 (NC_000010.10:107947265::TT 3418/3854) Row 28526896 (NC_000010.10:107947265::TTTTTTCTT 259/3854)	-	Oct 12, 2018 (152)
66	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 28526894 (NC_000010.10:107947265::TTTTTTT 157/3854) Row 28526895 (NC_000010.10:107947265::TT 3418/3854) Row 28526896 (NC_000010.10:107947265::TTTTTTCTT 259/3854)	-	Oct 12, 2018 (152)
67	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 28526894 (NC_000010.10:107947265::TTTTTTT 157/3854) Row 28526895 (NC_000010.10:107947265::TT 3418/3854) Row 28526896 (NC_000010.10:107947265::TTTTTTCTT 259/3854)	-	Oct 12, 2018 (152)
68	The Danish reference pan genome	NC_000010.10 - 107947266	Apr 26, 2020 (154)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 363016888 (NC_000010.11:106187507::TT 126424/129200) Row 363016889 (NC_000010.11:106187507::TTTTTTCTT 6/129252) Row 363016890 (NC_000010.11:106187507::TTTTTTT 2/129250)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 363016888 (NC_000010.11:106187507::TT 126424/129200) Row 363016889 (NC_000010.11:106187507::TTTTTTCTT 6/129252) Row 363016890 (NC_000010.11:106187507::TTTTTTT 2/129250)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 363016888 (NC_000010.11:106187507::TT 126424/129200) Row 363016889 (NC_000010.11:106187507::TTTTTTCTT 6/129252) Row 363016890 (NC_000010.11:106187507::TTTTTTT 2/129250)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 363016888 (NC_000010.11:106187507::TT 126424/129200) Row 363016889 (NC_000010.11:106187507::TTTTTTCTT 6/129252) Row 363016890 (NC_000010.11:106187507::TTTTTTT 2/129250)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 363016888 (NC_000010.11:106187507::TT 126424/129200) Row 363016889 (NC_000010.11:106187507::TTTTTTCTT 6/129252) Row 363016890 (NC_000010.11:106187507::TTTTTTT 2/129250)...	-	Apr 26, 2021 (155)
74	Northern Sweden	NC_000010.10 - 107947266	Jul 13, 2019 (153)
75	8.3KJPN Submission ignored due to conflicting rows: Row 57297206 (NC_000010.10:107947265::TT 16066/16756) Row 57297207 (NC_000010.10:107947265::TTT 12/16756)	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 57297206 (NC_000010.10:107947265::TT 16066/16756) Row 57297207 (NC_000010.10:107947265::TTT 12/16756)	-	Apr 26, 2021 (155)
77	14KJPN Submission ignored due to conflicting rows: Row 79492816 (NC_000010.11:106187507::TT 26026/27810) Row 79492817 (NC_000010.11:106187507::TTT 17/27810) Row 79492818 (NC_000010.11:106187507::T 1/27810)	-	Oct 13, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 79492816 (NC_000010.11:106187507::TT 26026/27810) Row 79492817 (NC_000010.11:106187507::TTT 17/27810) Row 79492818 (NC_000010.11:106187507::T 1/27810)	-	Oct 13, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 79492816 (NC_000010.11:106187507::TT 26026/27810) Row 79492817 (NC_000010.11:106187507::TTT 17/27810) Row 79492818 (NC_000010.11:106187507::T 1/27810)	-	Oct 13, 2022 (156)
80	UK 10K study - Twins Submission ignored due to conflicting rows: Row 28526894 (NC_000010.10:107947265::TTTTTTT 121/3708) Row 28526895 (NC_000010.10:107947265::TT 3416/3708) Row 28526896 (NC_000010.10:107947265::TTTTTTCTT 150/3708)	-	Oct 12, 2018 (152)
81	UK 10K study - Twins Submission ignored due to conflicting rows: Row 28526894 (NC_000010.10:107947265::TTTTTTT 121/3708) Row 28526895 (NC_000010.10:107947265::TT 3416/3708) Row 28526896 (NC_000010.10:107947265::TTTTTTCTT 150/3708)	-	Oct 12, 2018 (152)
82	UK 10K study - Twins Submission ignored due to conflicting rows: Row 28526894 (NC_000010.10:107947265::TTTTTTT 121/3708) Row 28526895 (NC_000010.10:107947265::TT 3416/3708) Row 28526896 (NC_000010.10:107947265::TTTTTTCTT 150/3708)	-	Oct 12, 2018 (152)
83	ALFA	NC_000010.11 - 106187508	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs68166393	Feb 27, 2009 (130)
rs140114381	May 15, 2013 (138)
rs141557404	May 11, 2012 (137)
rs142734827	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3007093543	NC_000010.10:107947265:TT:	NC_000010.11:106187507:TTTT:TT	(self)
ss4225019970	NC_000010.11:106187507:TT:	NC_000010.11:106187507:TTTT:TT	(self)
7615994134	NC_000010.11:106187507:TTTT:TT	NC_000010.11:106187507:TTTT:TT	(self)
ss5745655714	NC_000010.11:106187507::T	NC_000010.11:106187507:TTTT:TTTTT
7615994134	NC_000010.11:106187507:TTTT:TTTTT	NC_000010.11:106187507:TTTT:TTTTT	(self)
ss256137088, ss327276797, ss327359826, ss552065179, ss553426283	NC_000010.9:107937255::TT	NC_000010.11:106187507:TTTT:TTTTTT	(self)
ss294674925	NC_000010.9:107937258::TT	NC_000010.11:106187507:TTTT:TTTTTT	(self)
ss289035787	NC_000010.9:107937259::TT	NC_000010.11:106187507:TTTT:TTTTTT	(self)
51367706, 262960, 10935487, ss663949760, ss666514822, ss1370063358, ss1536667760, ss1574256501, ss1706887091, ss1706887244, ss2031041590, ss2627644719, ss3644306892, ss3737650622, ss3786778313, ss3791941818, ss3796823913, ss3832315061, ss5199327899, ss5650029573, ss5824913048, ss5980637086	NC_000010.10:107947265::TT	NC_000010.11:106187507:TTTT:TTTTTT	(self)
ss3063668226, ss3064490360, ss3065401538, ss3645160817, ss3813921375, ss4225019965, ss5285350641, ss5480785725, ss5745655712, ss5811856132, ss5849726512, ss5880389695	NC_000010.11:106187507::TT	NC_000010.11:106187507:TTTT:TTTTTT	(self)
7615994134	NC_000010.11:106187507:TTTT:TTTTTT	NC_000010.11:106187507:TTTT:TTTTTT	(self)
ss80839272, ss95551993, ss287865291	NT_030059.13:58751733::TT	NC_000010.11:106187507:TTTT:TTTTTT	(self)
ss3690616729	NC_000010.11:106187507::TTTTTTCT	NC_000010.11:106187507:TTTT:TTTTTT… NC_000010.11:106187507:TTTT:TTTTTTCTTTTT	(self)
ss3690616742	NC_000010.11:106187511::TTCTTTTT	NC_000010.11:106187507:TTTT:TTTTTT… NC_000010.11:106187507:TTTT:TTTTTTCTTTTT	(self)
ss1706887092, ss1706887247	NC_000010.10:107947265::TTTTTTCTT	NC_000010.11:106187507:TTTT:TTTTTT… NC_000010.11:106187507:TTTT:TTTTTTCTTTTTT	(self)
ss4225019966	NC_000010.11:106187507::TTTTTTCTT	NC_000010.11:106187507:TTTT:TTTTTT… NC_000010.11:106187507:TTTT:TTTTTTCTTTTTT	(self)
7615994134	NC_000010.11:106187507:TTTT:TTTTTT… NC_000010.11:106187507:TTTT:TTTTTTCTTTTTT	NC_000010.11:106187507:TTTT:TTTTTT… NC_000010.11:106187507:TTTT:TTTTTTCTTTTTT	(self)
ss3690616736	NC_000010.11:106187511::TTCTTTTTT	NC_000010.11:106187507:TTTT:TTTTTT… NC_000010.11:106187507:TTTT:TTTTTTCTTTTTT	(self)
ss3690616730	NC_000010.11:106187507::TTTTTTCTTTT	NC_000010.11:106187507:TTTT:TTTTTT… NC_000010.11:106187507:TTTT:TTTTTTCTTTTTTTT	(self)
ss5199327900	NC_000010.10:107947265::TTT	NC_000010.11:106187507:TTTT:TTTTTTT	(self)
ss5745655713	NC_000010.11:106187507::TTT	NC_000010.11:106187507:TTTT:TTTTTTT
ss3690616737, ss3690616743	NC_000010.11:106187511::TTT	NC_000010.11:106187507:TTTT:TTTTTTT	(self)
ss5824913050	NC_000010.10:107947265::TTTT	NC_000010.11:106187507:TTTT:TTTTTT… NC_000010.11:106187507:TTTT:TTTTTTTT
ss1706887089, ss1706887241, ss5824913052	NC_000010.10:107947265::TTTTTTT	NC_000010.11:106187507:TTTT:TTTTTT… NC_000010.11:106187507:TTTT:TTTTTTTTTTT	(self)
ss3690616731, ss4225019967	NC_000010.11:106187507::TTTTTTT	NC_000010.11:106187507:TTTT:TTTTTT… NC_000010.11:106187507:TTTT:TTTTTTTTTTT	(self)
ss5824913049	NC_000010.10:107947265::TTTTTTTT	NC_000010.11:106187507:TTTT:TTTTTT… NC_000010.11:106187507:TTTT:TTTTTTTTTTTT
ss4225019968	NC_000010.11:106187507::TTTTTTTTT	NC_000010.11:106187507:TTTT:TTTTTT… NC_000010.11:106187507:TTTT:TTTTTTTTTTTTT	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs68166392

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs68166392